Resource

Id	TF_ChIP-seq/ENCSR000BQTcontent_copy
Type	position_score
Version	0
Summary	TF_ChIP-seq ENCSR000BQT [biosample_summary="Homo sapiens GM12878" and target="TCF3"]
Description
Labels	accession: ENCSR000BQT assay_term_name: ChIP-seq biosample_ontology: /biosample-types/cell_line_EFO_0002784/ biosample_summary: Homo sapiens GM12878 date_created: 2013-09-13T16:54:09.860637-08:00 date_released: 2012-02-29 doi: 10.17989/ENCSR000BQT perturbed: False reference_genome: hg38/genomes/GRCh38-hg38 replication_type: isogenic simple_biosample_summary: status: released submitter_comment: target: TCF3

Scores (1)

ID	Type	Default annotation	Description	Histogram	Range	Summary
TF_ChIP-seq_ENCSR000BQT	float	TF_ChIP-seq_ENCSR000BQT	TF_ChIP-seq ENCSR000BQT [biosample_summary="Homo sapiens GM12878" and target="TCF3"]		[18.5, 397]	n 4,457,230 mean 36 sd 27.8

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

Chromosome	Covered positions	Covered %	Segments
all chromosomes	4457230	0.14%	16101
chr1	412387	0.17%	1484
chr2	331808	0.14%	1194
chr3	246303	0.12%	900
chr4	165629	0.09%	598
chr5	213453	0.12%	784
chr6	285074	0.17%	1013
chr7	213574	0.13%	771
chr8	172569	0.12%	628
chr9	180456	0.13%	651
chr10	196492	0.15%	716
chr11	223870	0.17%	812
chr12	218308	0.16%	792
chr13	94872	0.08%	342
chr14	149418	0.14%	547
chr15	141273	0.14%	507
chr16	225646	0.25%	800
chr17	269107	0.32%	975
chr18	78993	0.10%	285
chr19	250160	0.43%	904
chr20	133487	0.21%	481
chr21	69823	0.15%	247
chr22	113112	0.22%	409
chrX	71416	0.05%	261
3343 contigs with no values (186304500 bp)	0	0.00%	0

	segments	min	max	mean	median
segments	16101	3	1104	276.83	304