Resource

Id	TF_ChIP-seq/ENCSR000BGFcontent_copy
Type	position_score
Version	0
Summary	TF_ChIP-seq ENCSR000BGF [biosample_summary="Homo sapiens GM12878" and target="REST"]
Description
Labels	accession: ENCSR000BGF assay_term_name: ChIP-seq biosample_ontology: /biosample-types/cell_line_EFO_0002784/ biosample_summary: Homo sapiens GM12878 date_created: 2013-09-13T16:01:11.242290-08:00 date_released: 2011-07-18 doi: 10.17989/ENCSR000BGF perturbed: False reference_genome: hg38/genomes/GRCh38-hg38 replication_type: isogenic simple_biosample_summary: status: released submitter_comment: Fastq file ENCFF000NZA contains reads of mixed lengths. Read lengths followed by respective number of reads: (32, 32310422), (36, 27398933). target: REST

Scores (1)

ID	Type	Default annotation	Description	Histogram	Range	Summary
TF_ChIP-seq_ENCSR000BGF	float	TF_ChIP-seq_ENCSR000BGF	TF_ChIP-seq ENCSR000BGF [biosample_summary="Homo sapiens GM12878" and target="REST"]		[3.24, 457]	n 1,338,178 mean 105 sd 117

n counts base pairs; sd is the population standard deviation.

Chromosome	Covered positions	Covered %	Segments
all chromosomes	1338178	0.04%	5735
chr1	128802	0.05%	545
chr2	99074	0.04%	429
chr3	80938	0.04%	342
chr4	43300	0.02%	191
chr5	68672	0.04%	297
chr6	67966	0.04%	295
chr7	60281	0.04%	263
chr8	58561	0.04%	251
chr9	54263	0.04%	230
chr10	65494	0.05%	284
chr11	76821	0.06%	333
chr12	67091	0.05%	287
chr13	24841	0.02%	111
chr14	38868	0.04%	165
chr15	44907	0.04%	193
chr16	56572	0.06%	246
chr17	68454	0.08%	293
chr18	27968	0.03%	124
chr19	82343	0.14%	335
chr20	54147	0.08%	226
chr21	9547	0.02%	42
chr22	33378	0.07%	141
chrX	25890	0.02%	112
3343 contigs with no values (186304500 bp)	0	0.00%	0

	segments	min	max	mean	median
segments	5735	1	672	233.34	236