Resource

Id	TF_ChIP-seq/ENCSR000BQVcontent_copy
Type	position_score
Version	0
Summary	TF_ChIP-seq ENCSR000BQV [biosample_summary="Homo sapiens H1" and target="SP4"]
Description
Labels	accession: ENCSR000BQV assay_term_name: ChIP-seq biosample_ontology: /biosample-types/cell_line_EFO_0003042/ biosample_summary: Homo sapiens H1 date_created: 2013-12-12T06:33:10.651750+00:00 date_released: 2012-02-29 doi: 10.17989/ENCSR000BQV perturbed: False reference_genome: hg38/genomes/GRCh38-hg38 replication_type: isogenic simple_biosample_summary: status: released submitter_comment: target: SP4

Scores (1)

ID	Type	Default annotation	Description	Histogram	Range	Summary
TF_ChIP-seq_ENCSR000BQV	float	TF_ChIP-seq_ENCSR000BQV	TF_ChIP-seq ENCSR000BQV [biosample_summary="Homo sapiens H1" and target="SP4"]		[32.9, 478]	n 3,236,001 mean 47.9 sd 32.7

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

Chromosome	Covered positions	Covered %	Segments
all chromosomes	3236001	0.10%	6137
chr1	361215	0.15%	686
chr2	196501	0.08%	371
chr3	169458	0.09%	311
chr4	102448	0.05%	190
chr5	134664	0.07%	245
chr6	183740	0.11%	339
chr7	157866	0.10%	289
chr8	93476	0.06%	174
chr9	123804	0.09%	235
chr10	124532	0.09%	233
chr11	191426	0.14%	360
chr12	182086	0.14%	347
chr13	51026	0.04%	92
chr14	93813	0.09%	177
chr15	101779	0.10%	192
chr16	162872	0.18%	315
chr17	215788	0.26%	412
chr18	28308	0.04%	51
chr19	355530	0.61%	726
chr20	89628	0.14%	164
chr21	25962	0.06%	52
chr22	67069	0.13%	132
chrX	23010	0.01%	44
3343 contigs with no values (186304500 bp)	0	0.00%	0

	segments	min	max	mean	median
segments	6137	2	1202	527.29	610