Variant report

Variant	rs3807803
Chromosome Location	chr7:8300728-8300729
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	MAX	chr7:8300432-8302566	MCF-7	breast:	n/a	chr7:8300605-8300614
2	MYC	chr7:8300538-8301068	MCF10A-Er-Src	breast:	n/a	chr7:8300605-8300614
3	UBTF	chr7:8300467-8302342	K562	blood:	n/a	n/a
4	FOS	chr7:8300228-8302669	HUVEC	blood vessel:	n/a	chr7:8300607-8300614 chr7:8300606-8300615 chr7:8300605-8300614 chr7:8300604-8300615 chr7:8300606-8300614
5	POLR2A	chr7:8300721-8302460	HCT-116	colon:	n/a	n/a
6	MXI1	chr7:8298200-8304061	SK-N-SH	brain:	n/a	n/a
7	EP300	chr7:8300180-8301212	K562	blood:	n/a	chr7:8300605-8300614 chr7:8300606-8300615
8	JUND	chr7:8300433-8300785	HepG2	liver:	n/a	chr7:8300607-8300614 chr7:8300606-8300615 chr7:8300604-8300615 chr7:8300605-8300614 chr7:8300606-8300614
9	SIN3AK20	chr7:8300471-8302542	MCF-7	breast:	n/a	n/a
10	MYC	chr7:8300533-8302414	K562	blood:	n/a	chr7:8300605-8300614
11	FOSL2	chr7:8300321-8300906	MCF-7	breast:	n/a	chr7:8300607-8300614 chr7:8300606-8300615 chr7:8300605-8300614 chr7:8300606-8300614
12	PML	chr7:8300593-8301286	K562	blood:	n/a	chr7:8300604-8300613
13	JUN	chr7:8300478-8300869	K562	blood:	n/a	chr7:8300607-8300614 chr7:8300606-8300615 chr7:8300605-8300614 chr7:8300606-8300614
14	CHD2	chr7:8300533-8300829	K562	blood:	n/a	n/a
15	FOS	chr7:8300434-8300764	MCF10A-Er-Src	breast:	n/a	chr7:8300607-8300614 chr7:8300606-8300615 chr7:8300605-8300614 chr7:8300604-8300615 chr7:8300606-8300614
16	ARID3A	chr7:8300420-8300901	K562	blood:	n/a	n/a
17	POLR2A	chr7:8300685-8301347	HUVEC	blood vessel:	n/a	n/a
18	CUX1	chr7:8300396-8300806	K562	blood:	n/a	n/a
19	FOSL2	chr7:8300365-8300760	MCF-7	breast:	n/a	chr7:8300607-8300614 chr7:8300606-8300615 chr7:8300605-8300614 chr7:8300606-8300614
20	POLR2A	chr7:8300488-8302512	MCF10A-Er-Src	breast:	n/a	n/a
21	JUND	chr7:8300373-8302543	K562	blood:	n/a	chr7:8300607-8300614 chr7:8300606-8300615 chr7:8300604-8300615 chr7:8300605-8300614 chr7:8300606-8300614
22	BHLHE40	chr7:8300597-8301032	K562	blood:	n/a	n/a
23	TBP	chr7:8300588-8302460	K562	blood:	n/a	n/a
24	EP300	chr7:8297240-8304935	SK-N-SH	brain:	n/a	chr7:8301242-8301256 chr7:8302651-8302665 chr7:8302093-8302106 chr7:8303194-8303204 chr7:8300605-8300614 chr7:8303165-8303175 chr7:8301853-8301862 chr7:8300606-8300615 chr7:8301597-8301613 chr7:8301595-8301604
25	POLR2A	chr7:8300559-8302141	HUVEC	blood vessel:	n/a	n/a
26	FOS	chr7:8300448-8301064	MCF10A-Er-Src	breast:	n/a	chr7:8300607-8300614 chr7:8300606-8300615 chr7:8300605-8300614 chr7:8300604-8300615 chr7:8300606-8300614
27	POLR2A	chr7:8300545-8302215	HUVEC	blood vessel:	n/a	n/a
28	JUND	chr7:8300300-8303202	SK-N-SH	brain:	n/a	chr7:8300607-8300614 chr7:8300606-8300615 chr7:8300604-8300615 chr7:8300605-8300614 chr7:8300606-8300614
29	BRCA1	chr7:8300690-8300975	Hela-S3	cervix:	n/a	n/a
30	GABPA	chr7:8300546-8302186	MCF-7	breast:	n/a	chr7:8301595-8301604
31	POLR2A	chr7:8300062-8302108	K562	blood:	n/a	n/a
32	RFX5	chr7:8300560-8301954	Hela-S3	cervix:	n/a	n/a
33	FOS	chr7:8300202-8301002	MCF10A-Er-Src	breast:	n/a	chr7:8300607-8300614 chr7:8300606-8300615 chr7:8300605-8300614 chr7:8300604-8300615 chr7:8300606-8300614
34	FOS	chr7:8300428-8300744	MCF10A-Er-Src	breast:	n/a	chr7:8300607-8300614 chr7:8300606-8300615 chr7:8300605-8300614 chr7:8300604-8300615 chr7:8300606-8300614
35	ZNF263	chr7:8300514-8302247	HEK293-T-REx	kidney:	n/a	chr7:8301514-8301535 chr7:8301516-8301525
36	TBP	chr7:8300626-8301137	Hela-S3	cervix:	n/a	n/a
37	POLR2A	chr7:8300640-8302113	HUVEC	blood vessel:	n/a	n/a
38	POLR2A	chr7:8300427-8302077	HUVEC	blood vessel:	n/a	n/a
39	POLR2A	chr7:8300642-8302294	K562	blood:	n/a	n/a
40	MAFK	chr7:8300360-8301195	K562	blood:	n/a	chr7:8300604-8300613 chr7:8301044-8301054
41	POLR2A	chr7:8300584-8302338	Hela-S3	cervix:	n/a	n/a
42	MYC	chr7:8300655-8302449	K562	blood:	n/a	n/a
43	POLR2A	chr7:8300230-8302412	PBDE	blood:	n/a	n/a
44	POLR2A	chr7:8300508-8302409	K562	blood:	n/a	n/a
45	JUN	chr7:8300424-8300942	HUVEC	blood vessel:	n/a	chr7:8300607-8300614 chr7:8300606-8300615 chr7:8300605-8300614 chr7:8300606-8300614
46	POLR2A	chr7:8300376-8301110	SK-N-SH	brain:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:8300728-8300778	HepG2	liver:	n/a
2	chr7:8300728-8300778	ProgFib	skin:	n/a
3	chr7:8300728-8300778	H1-hESC	embryonic stem cell:	embryo
4	chr7:8300728-8300778	PrEC	prostate:	n/a
5	chr7:8300728-8300778	AG04450	lung:	fetal
6	chr7:8300728-8300778	CMK	blood:	n/a
7	chr7:8300728-8300778	T-47D	breast:	n/a
8	chr7:8300728-8300778	HPAEpiC	pulmonary alveolar:	n/a
9	chr7:8300728-8300778	HRPEpiC	eye:	n/a
10	chr7:8300728-8300778	BJ	skin:	n/a
11	chr7:8300728-8300778	NT2-D1	testis:	n/a
12	chr7:8300728-8300778	AG10803	skin:	n/a
13	chr7:8300728-8300778	MCF-7	breast:	n/a
14	chr7:8300728-8300778	Hela-S3	cervix:	n/a
15	chr7:8300728-8300778	SAEC	small airway:	n/a
16	chr7:8300728-8300778	HMEC	breast:	n/a
17	chr7:8300728-8300778	HCM	heart:	n/a
18	chr7:8300728-8300778	PFSK-1	brain:	n/a
19	chr7:8300728-8300778	SKMC	muscle:	n/a
20	chr7:8300728-8300778	IMR90	lung:	fetal
21	chr7:8300728-8300778	HNPCEpiC	eye:	n/a
22	chr7:8300728-8300778	HCPEpiC	choroid plexus:	n/a
23	chr7:8300728-8300778	HRE	kidney:	n/a
24	chr7:8300728-8300778	AoSMC	blood vessel:	n/a
25	chr7:8300728-8300778	PANC-1	pancreas:	n/a
26	chr7:8300728-8300778	HCT-116	colon:	n/a
27	chr7:8300728-8300778	NHBE	bronchial:	n/a
28	chr7:8300728-8300778	SK-N-SH	brain:	n/a
29	chr7:8300728-8300778	GM12878	blood:	n/a
30	chr7:8300728-8300778	HL-60	blood:	n/a
31	chr7:8300728-8300778	Jurkat	blood:	n/a
32	chr7:8300728-8300778	HRCEpiC	kidney:	n/a
33	chr7:8300728-8300778	AG09309	skin:	n/a
34	chr7:8300728-8300778	GM12892	blood:	n/a
35	chr7:8300728-8300778	BE2_C	brain:	n/a
36	chr7:8300728-8300778	K562	blood:	n/a
37	chr7:8300728-8300778	MCF10A-Er-Src	breast:	n/a
38	chr7:8300728-8300778	GM12891	blood:	n/a
39	chr7:8300728-8300778	A549	lung:	n/a
40	chr7:8300728-8300778	HUVEC	blood vessel:	n/a
41	chr7:8300728-8300778	SK-N-MC	brain:	n/a
42	chr7:8300728-8300778	Hepatocyte	liver:	n/a
43	chr7:8300728-8300778	HAEpiC	amniotic membrane:	n/a
44	chr7:8300728-8300778	HEEpiC	esophagus:	n/a
45	chr7:8300728-8300778	HEK293	kidney:	embryo
46	chr7:8300728-8300778	GM06990	blood:	n/a
47	chr7:8300728-8300778	ovcar-3	ovarian:	n/a
48	chr7:8300728-8300778	Caco-2	colon:	n/a
49	chr7:8300728-8300778	HIPEpiC	eye:	n/a
50	chr7:8300728-8300778	AG04449	skin:	fetal

No.	Distal block	Cell Line	Cell type
1	chr7:7678479..7681346-chr7:8300009..8302111,2	K562	blood:
2	chr16:18812683..18814346-chr7:8299005..8301772,2	MCF-7	breast:
3	chr7:8272591..8276389-chr7:8300036..8303147,3	MCF-7	breast:
4	chr7:7978772..7980836-chr7:8298772..8301162,2	K562	blood:
5	chr7:8298736..8301504-chr7:8417634..8420051,2	K562	blood:
6	chr7:7601559..7604327-chr7:8300528..8302351,2	MCF-7	breast:
7	chr7:8284762..8287625-chr7:8298919..8300747,2	MCF-7	breast:
8	chr7:8299069..8300796-chr7:8446906..8448804,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000229970	TF binding region
ENSG00000244239	TF binding region
ENSG00000244239	CpG island
ENSG00000229970	CpG island
ENSG00000260342	Chromatin interaction
ENSG00000003147	Chromatin interaction
ENSG00000170540	Chromatin interaction
ENSG00000272894	Chromatin interaction
ENSG00000219545	Chromatin interaction
ENSG00000106399	Chromatin interaction

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs11769978	0.82[ASN][1000 genomes]
rs2302551	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3779356	0.95[ASN][1000 genomes]
rs3779357	0.94[ASN][1000 genomes]
rs3807801	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3807802	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3807804	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3807806	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3807807	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3807808	0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3807809	0.82[ASN][1000 genomes]
rs3807810	0.92[ASN][1000 genomes]
rs3823815	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3823816	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9472	0.81[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:24 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv917172	chr7:7854632-8807385	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
2	nsv1020686	chr7:8095118-8311985	Enhancers Strong transcription Flanking Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
3	nsv538723	chr7:8095118-8311985	Weak transcription Strong transcription Enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
4	nsv949024	chr7:8176301-8522495	Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
5	nsv1031226	chr7:8176311-8569811	Bivalent Enhancer Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
6	nsv538724	chr7:8176311-8569811	Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
7	nsv887492	chr7:8177689-8513927	Flanking Active TSS Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
8	nsv1026247	chr7:8178837-8527868	Weak transcription ZNF genes & repeats Bivalent Enhancer Strong transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
9	nsv464305	chr7:8179655-8524707	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
10	nsv606050	chr7:8179655-8524707	Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
11	nsv1020942	chr7:8179655-8524774	Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
12	nsv464307	chr7:8179846-8453313	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
13	nsv606051	chr7:8179846-8453313	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
14	nsv1034583	chr7:8180210-8527868	Bivalent Enhancer Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
15	nsv1030373	chr7:8184961-8527868	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Active TSS Bivalent/Poised TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
16	nsv949082	chr7:8189594-8494386	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
17	nsv948997	chr7:8189594-8522495	Weak transcription Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
18	nsv915625	chr7:8201631-8554402	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
19	nsv1033563	chr7:8222805-8512632	Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Strong transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
20	nsv1024586	chr7:8243829-8490078	Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
21	nsv538725	chr7:8243829-8490078	Bivalent Enhancer Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
22	nsv949715	chr7:8288705-8522495	Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
23	nsv464308	chr7:8288705-8953858	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Enhancers Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
24	nsv606054	chr7:8288705-8953858	Enhancers Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:85 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:8289000-8300800	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr7:8294800-8300800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr7:8294800-8300800	Weak transcription	Gastric	stomach
4	chr7:8296200-8300800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr7:8296400-8300800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr7:8296600-8300800	Weak transcription	Lung	lung
7	chr7:8299000-8300800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr7:8299800-8301200	Active TSS	Right Atrium	heart
9	chr7:8300000-8301000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr7:8300000-8301200	Flanking Active TSS	Primary hematopoietic stem cells	blood
11	chr7:8300000-8302200	Active TSS	Brain Angular Gyrus	brain
12	chr7:8300000-8302600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
13	chr7:8300000-8302600	Active TSS	Right Ventricle	heart
14	chr7:8300000-8304000	Active TSS	Pancreatic Islets	Pancreatic Islet
15	chr7:8300200-8300800	Active TSS	Fetal Stomach	stomach
16	chr7:8300200-8301000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr7:8300200-8302000	Active TSS	Fetal Intestine Large	intestine
18	chr7:8300200-8302200	Active TSS	K562	blood
19	chr7:8300200-8302800	Active TSS	Rectal Mucosa Donor 29	rectum
20	chr7:8300400-8300800	Active TSS	Fetal Adrenal Gland	Adrenal Gland
21	chr7:8300400-8300800	Bivalent/Poised TSS	Fetal Brain Male	brain
22	chr7:8300400-8301000	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr7:8300400-8301000	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr7:8300400-8301000	Flanking Active TSS	Hela-S3	cervix
25	chr7:8300400-8301000	Flanking Active TSS	HUVEC	blood vessel
26	chr7:8300400-8301000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
27	chr7:8300400-8301400	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr7:8300400-8302000	Active TSS	Brain Hippocampus Middle	brain
29	chr7:8300400-8302000	Active TSS	NHEK	skin
30	chr7:8300400-8302200	Active TSS	Brain Inferior Temporal Lobe	brain
31	chr7:8300400-8302200	Bivalent/Poised TSS	Fetal Brain Female	brain
32	chr7:8300400-8302200	Bivalent/Poised TSS	Psoas Muscle	Psoas
33	chr7:8300400-8302200	Active TSS	Stomach Mucosa	stomach
34	chr7:8300400-8302400	Active TSS	Fetal Intestine Small	intestine
35	chr7:8300400-8302600	Active TSS	Brain Cingulate Gyrus	brain
36	chr7:8300400-8302800	Active TSS	Duodenum Mucosa	Duodenum
37	chr7:8300400-8302800	Active TSS	Rectal Mucosa Donor 31	rectum
38	chr7:8300600-8300800	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
39	chr7:8300600-8300800	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
40	chr7:8300600-8300800	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
41	chr7:8300600-8300800	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
42	chr7:8300600-8300800	Bivalent/Poised TSS	Primary B cells from cord blood	blood
43	chr7:8300600-8300800	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
44	chr7:8300600-8300800	Enhancers	Cortex derived primary cultured neurospheres	brain
45	chr7:8300600-8300800	Bivalent/Poised TSS	Adipose Nuclei	Adipose
46	chr7:8300600-8300800	Flanking Active TSS	Brain Substantia Nigra	brain
47	chr7:8300600-8300800	Active TSS	Placenta	Placenta
48	chr7:8300600-8300800	Active TSS	Rectal Smooth Muscle	rectum
49	chr7:8300600-8300800	Flanking Bivalent TSS/Enh	A549	lung
50	chr7:8300600-8300800	Active TSS	NH-A	brain

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