Resource

Id	TF_ChIP-seq/ENCSR000BSFcontent_copy
Type	position_score
Version	0
Summary	TF_ChIP-seq ENCSR000BSF [biosample_summary="Homo sapiens HCT116" and target="SP1"]
Description
Labels	accession: ENCSR000BSF assay_term_name: ChIP-seq biosample_ontology: /biosample-types/cell_line_EFO_0002824/ biosample_summary: Homo sapiens HCT116 date_created: 2013-12-19T20:51:47.570447+00:00 date_released: 2012-09-10 doi: 10.17989/ENCSR000BSF perturbed: False reference_genome: hg38/genomes/GRCh38-hg38 replication_type: isogenic simple_biosample_summary: status: released submitter_comment: target: SP1

Scores (1)

ID	Type	Default annotation	Description	Histogram	Range	Summary
TF_ChIP-seq_ENCSR000BSF	float	TF_ChIP-seq_ENCSR000BSF	TF_ChIP-seq ENCSR000BSF [biosample_summary="Homo sapiens HCT116" and target="SP1"]		[5.82, 516]	n 11,716,566 mean 62.2 sd 55.8

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

Chromosome	Covered positions	Covered %	Segments
all chromosomes	11716566	0.36%	33944
chr1	1169114	0.47%	3459
chr2	978467	0.40%	2839
chr3	737000	0.37%	2135
chr4	656798	0.35%	1900
chr5	561683	0.31%	1604
chr6	818698	0.48%	2407
chr7	596222	0.37%	1689
chr8	548431	0.38%	1626
chr9	415652	0.30%	1206
chr10	612707	0.46%	1770
chr11	566300	0.42%	1627
chr12	671170	0.50%	1959
chr13	189060	0.17%	532
chr14	327884	0.31%	962
chr15	316946	0.31%	871
chr16	361669	0.40%	1039
chr17	619547	0.74%	1780
chr18	201255	0.25%	590
chr19	566701	0.97%	1707
chr20	290641	0.45%	821
chr21	70449	0.15%	198
chr22	205409	0.40%	583
chrX	234327	0.15%	639
chrY	436	<0.01%	1
3342 contigs with no values (129077085 bp)	0	0.00%	0

	segments	min	max	mean	median
segments	33944	1	770	345.17	436