Variant report

Variant	rs7629917
Chromosome Location	chr3:50358464-50358465
allele	C/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	POLR2A	chr3:50358463-50358647	A549	lung:	n/a	n/a
2	POLR2A	chr3:50358167-50359756	HepG2	liver:	n/a	n/a
3	TCF12	chr3:50358336-50359499	A549	lung:	n/a	n/a
4	TCF7L2	chr3:50358452-50359309	Hela-S3	cervix:	n/a	n/a
5	JUND	chr3:50357854-50359828	SK-N-SH	brain:	n/a	chr3:50359247-50359256 chr3:50359250-50359259 chr3:50359440-50359449 chr3:50359131-50359143 chr3:50359090-50359104 chr3:50359249-50359258 chr3:50359248-50359257 chr3:50358457-50358471
6	POLR2A	chr3:50358047-50359278	MCF10A-Er-Src	breast:	n/a	n/a
7	POLR2A	chr3:50358333-50359024	K562	blood:	n/a	n/a
8	MAX	chr3:50358223-50359330	Hela-S3	cervix:	n/a	chr3:50358671-50358680
9	POLR2A	chr3:50358329-50359026	SK-N-SH	brain:	n/a	n/a
10	EP300	chr3:50358429-50359340	H1-hESC	embryonic stem cell:	n/a	chr3:50359191-50359200 chr3:50359183-50359199 chr3:50359182-50359198
11	CHD2	chr3:50358341-50359775	HepG2	liver:	n/a	chr3:50358596-50358606 chr3:50358794-50358804
12	POLR2A	chr3:50358350-50359030	Hela-S3	cervix:	n/a	n/a
13	MAZ	chr3:50358349-50359571	GM12878	blood:	n/a	chr3:50359499-50359509 chr3:50358671-50358680
14	POLR2A	chr3:50358170-50360519	HUVEC	blood vessel:	n/a	n/a
15	TCF12	chr3:50358271-50359564	ECC-1	luminal epithelium:	n/a	n/a
16	MXI1	chr3:50358173-50359370	Hela-S3	cervix:	n/a	n/a
17	SP1	chr3:50358389-50359486	GM12878	blood:	n/a	chr3:50359439-50359448 chr3:50358654-50358663 chr3:50358660-50358669 chr3:50358693-50358707 chr3:50359438-50359452 chr3:50358654-50358664 chr3:50358907-50358916 chr3:50358906-50358915 chr3:50359437-50359449 chr3:50358975-50358986 chr3:50358654-50358663 chr3:50358655-50358664 chr3:50358697-50358707 chr3:50358661-50358670 chr3:50358659-50358671 chr3:50358441-50358454 chr3:50358697-50358706 chr3:50359438-50359447 chr3:50358905-50358917 chr3:50358653-50358665 chr3:50358659-50358671 chr3:50358654-50358664 chr3:50358520-50358527 chr3:50358905-50358917 chr3:50358906-50358920 chr3:50358653-50358665
18	POLR2A	chr3:50358293-50359203	U87	brain:	n/a	n/a
19	CTCF	chr3:50358460-50358610	GM12878	blood:	n/a	n/a
20	MAX	chr3:50358380-50359438	MCF-7	breast:	n/a	chr3:50358671-50358680
21	CREB1	chr3:50358439-50359233	A549	lung:	n/a	n/a
22	JUN	chr3:50358371-50359452	K562	blood:	n/a	chr3:50359247-50359256 chr3:50359250-50359259 chr3:50359440-50359449 chr3:50359131-50359143 chr3:50359090-50359104 chr3:50359249-50359258 chr3:50359248-50359257 chr3:50358457-50358471
23	POLR2A	chr3:50358364-50359484	MCF-7	breast:	n/a	n/a
24	SP1	chr3:50357949-50359619	HCT-116	colon:	n/a	chr3:50359439-50359448 chr3:50358654-50358663 chr3:50358660-50358669 chr3:50358693-50358707 chr3:50359438-50359452 chr3:50359493-50359507 chr3:50358654-50358664 chr3:50358907-50358916 chr3:50359492-50359504 chr3:50358906-50358915 chr3:50359493-50359502 chr3:50359437-50359449 chr3:50358975-50358986 chr3:50358654-50358663 chr3:50358655-50358664 chr3:50358697-50358707 chr3:50359492-50359504 chr3:50358661-50358670 chr3:50358659-50358671 chr3:50359493-50359503 chr3:50358441-50358454 chr3:50358697-50358706 chr3:50359438-50359447 chr3:50358905-50358917 chr3:50358653-50358665 chr3:50359493-50359502 chr3:50359494-50359503 chr3:50358659-50358671 chr3:50358654-50358664 chr3:50358520-50358527 chr3:50358905-50358917 chr3:50358906-50358920 chr3:50358653-50358665 chr3:50359493-50359503
25	SIN3AK20	chr3:50358322-50359015	K562	blood:	n/a	n/a
26	EP300	chr3:50358451-50359499	SK-N-SH	brain:	n/a	chr3:50359191-50359200 chr3:50359183-50359199 chr3:50359182-50359198
27	POLR2A	chr3:50358223-50362338	HUVEC	blood vessel:	n/a	n/a
28	POLR2A	chr3:50358309-50359240	Hela-S3	cervix:	n/a	n/a
29	POLR2A	chr3:50358105-50360508	H1-hESC	embryonic stem cell:	n/a	n/a
30	STAT3	chr3:50358385-50358645	MCF10A-Er-Src	breast:	n/a	n/a
31	SMC3	chr3:50358143-50359411	Hela-S3	cervix:	n/a	chr3:50359319-50359329 chr3:50358909-50358919
32	CHD2	chr3:50358232-50359456	K562	blood:	n/a	chr3:50358596-50358606 chr3:50358794-50358804
33	POLR2A	chr3:50357990-50359301	MCF10A-Er-Src	breast:	n/a	n/a
34	POLR2A	chr3:50353534-50362749	HUVEC	blood vessel:	n/a	n/a
35	POLR2A	chr3:50358342-50359063	U87	brain:	n/a	n/a
36	POLR2A	chr3:50358369-50359473	K562	blood:	n/a	n/a
37	MXI1	chr3:50358346-50359127	K562	blood:	n/a	n/a
38	UBTF	chr3:50358081-50358915	K562	blood:	n/a	n/a
39	HCFC1	chr3:50358154-50359603	Hela-S3	cervix:	n/a	n/a
40	REST	chr3:50357851-50359910	H1-neurons	neurons:	n/a	chr3:50359493-50359506
41	USF1	chr3:50358413-50358940	ECC-1	luminal epithelium:	n/a	n/a
42	POLR2A	chr3:50358210-50359663	GM12891	blood:	n/a	n/a
43	EP300	chr3:50357984-50359591	ECC-1	luminal epithelium:	n/a	chr3:50359191-50359200 chr3:50359183-50359199 chr3:50359182-50359198
44	JUND	chr3:50358109-50359646	GM12878	blood:	n/a	chr3:50359247-50359256 chr3:50359250-50359259 chr3:50359440-50359449 chr3:50359131-50359143 chr3:50359090-50359104 chr3:50359249-50359258 chr3:50359248-50359257 chr3:50358457-50358471
45	KAP1	chr3:50358401-50359467	U2OS	brain:	n/a	n/a
46	POLR2A	chr3:50358164-50359580	H1-neurons	neurons:	n/a	n/a
47	TAF1	chr3:50358452-50358712	K562	blood:	n/a	n/a
48	SIN3A	chr3:50358047-50360497	H1-hESC	embryonic stem cell:	n/a	chr3:50358629-50358640 chr3:50359896-50359909 chr3:50360384-50360397 chr3:50358604-50358615 chr3:50359295-50359303 chr3:50360182-50360195
49	MYC	chr3:50358343-50359533	NB4	blood:	n/a	chr3:50359499-50359509 chr3:50358671-50358680
50	POLR2A	chr3:50358304-50359773	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:50358443-50358493	AG04449	skin:	fetal
2	chr3:50358443-50358493	Hepatocyte	liver:	n/a
3	chr3:50358443-50358493	SAEC	small airway:	n/a
4	chr3:50358443-50358493	NT2-D1	testis:	n/a
5	chr3:50358443-50358493	NB4	blood:	n/a
6	chr3:50358443-50358493	MCF10A-Er-Src	breast:	n/a
7	chr3:50358443-50358493	HRE	kidney:	n/a
8	chr3:50358443-50358493	AG09319	gingival:	n/a
9	chr3:50358443-50358493	HIPEpiC	eye:	n/a
10	chr3:50358443-50358493	HCT-116	colon:	n/a
11	chr3:50358443-50358493	HEEpiC	esophagus:	n/a
12	chr3:50358443-50358493	Caco-2	colon:	n/a
13	chr3:50358443-50358493	HCM	heart:	n/a
14	chr3:50358443-50358493	SK-N-MC	brain:	n/a
15	chr3:50358443-50358493	HMEC	breast:	n/a
16	chr3:50358443-50358493	HL-60	blood:	n/a
17	chr3:50358443-50358493	AG10803	skin:	n/a
18	chr3:50358443-50358493	RPTEC	kidney:	n/a
19	chr3:50358443-50358493	K562	blood:	n/a
20	chr3:50358443-50358493	HEK293	kidney:	embryo
21	chr3:50358443-50358493	SK-N-SH	brain:	n/a
22	chr3:50358443-50358493	GM12892	blood:	n/a
23	chr3:50358443-50358493	HepG2	liver:	n/a
24	chr3:50358443-50358493	ovcar-3	ovarian:	n/a
25	chr3:50358443-50358493	HPAEpiC	pulmonary alveolar:	n/a
26	chr3:50358443-50358493	SK-N-SH_RA	brain:	n/a
27	chr3:50358443-50358493	MCF-7	breast:	n/a
28	chr3:50358443-50358493	HNPCEpiC	eye:	n/a
29	chr3:50358443-50358493	HRCEpiC	kidney:	n/a
30	chr3:50358443-50358493	AoSMC	blood vessel:	n/a
31	chr3:50358443-50358493	A549	lung:	n/a
32	chr3:50358443-50358493	BE2_C	brain:	n/a
33	chr3:50358443-50358493	Jurkat	blood:	n/a
34	chr3:50358443-50358493	U87	brain:	n/a
35	chr3:50358443-50358493	PFSK-1	brain:	n/a
36	chr3:50358443-50358493	H1-hESC	embryonic stem cell:	embryo
37	chr3:50358443-50358493	AG04450	lung:	fetal
38	chr3:50358443-50358493	AG09309	skin:	n/a
39	chr3:50358443-50358493	GM12891	blood:	n/a
40	chr3:50358443-50358493	Hela-S3	cervix:	n/a
41	chr3:50358443-50358493	GM12878	blood:	n/a
42	chr3:50358443-50358493	CMK	blood:	n/a
43	chr3:50358443-50358493	SKMC	muscle:	n/a
44	chr3:50358443-50358493	ProgFib	skin:	n/a
45	chr3:50358443-50358493	LNCaP	prostate:	n/a
46	chr3:50358443-50358493	GM19239	blood:	n/a
47	chr3:50358443-50358493	NH-A	brain:	n/a
48	chr3:50358443-50358493	HRPEpiC	eye:	n/a
49	chr3:50358443-50358493	GM06990	blood:	n/a
50	chr3:50358443-50358493	HCF	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:50324564..50342616-chr3:50350801..50362499,49	MCF-7	breast:
2	chr3:50327926..50342388-chr3:50350886..50359960,36	MCF-7	breast:
3	chr3:50286473..50289840-chr3:50357894..50361890,3	MCF-7	breast:
4	chr16:699274..699844-chr3:50358088..50358911,2	Hela-S3	cervix:
5	chr3:50300460..50314689-chr3:50349154..50363682,34	MCF-7	breast:
6	chr3:50357006..50359780-chr3:50383259..50385095,2	MCF-7	breast:
7	chr3:50314390..50316856-chr3:50357107..50359753,2	MCF-7	breast:
8	chr3:50273339..50275012-chr3:50356233..50359158,2	K562	blood:
9	chr3:50295790..50299500-chr3:50356173..50362991,11	MCF-7	breast:
10	chr3:50296091..50300659-chr3:50356103..50362246,11	MCF-7	breast:
11	chr3:50334885..50342502-chr3:50352987..50366859,26	K562	blood:
12	chr3:50307238..50313479-chr3:50353130..50365794,18	MCF-7	breast:
13	chr3:50273482..50276230-chr3:50357348..50359283,2	MCF-7	breast:
14	chr3:50356822..50362778-chr3:50372728..50378128,10	MCF-7	breast:
15	chr3:50315023..50318386-chr3:50356939..50360295,5	MCF-7	breast:
16	chr3:50309725..50313756-chr3:50357883..50363910,8	K562	blood:
17	chr3:50326497..50331702-chr3:50356299..50362839,8	K562	blood:
18	chr3:50334334..50341950-chr3:50357130..50360296,11	K562	blood:
19	chr3:50357891..50360438-chr3:50381704..50384677,2	MCF-7	breast:

Variant related genes	Relation type
HYAL2	TF binding region
HYAL2	CpG island
ENSG00000004838	Chromatin interaction
ENSG00000012171	Chromatin interaction
ENSG00000186792	Chromatin interaction
ENSG00000230454	Chromatin interaction
ENSG00000232352	Chromatin interaction
ENSG00000114353	Chromatin interaction
ENSG00000161996	Chromatin interaction
ENSG00000179564	Chromatin interaction
ENSG00000068028	Chromatin interaction
ENSG00000214706	Chromatin interaction
ENSG00000114378	Chromatin interaction
ENSG00000243477	Chromatin interaction

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs11914549	0.83[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11916258	0.86[AMR][1000 genomes]
rs35742391	0.95[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs56287038	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57453427	0.90[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs58415636	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61382127	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6446203	0.86[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6768830	0.90[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7641224	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs886075	0.95[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs9851719	0.82[EUR][1000 genomes]
rs9875873	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs9878345	0.82[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:21 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv523662	chr3:50144951-50584999	Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	101 gene(s)	inside rSNPs	diseases
2	nsv876769	chr3:50155468-50408398	Active TSS Enhancers Weak transcription Genic enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	94 gene(s)	inside rSNPs	diseases
3	esv1821728	chr3:50156142-50657253	Strong transcription Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	109 gene(s)	inside rSNPs	diseases
4	esv1793751	chr3:50157364-50476363	Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	98 gene(s)	inside rSNPs	diseases
5	esv1828162	chr3:50157364-50506151	Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	98 gene(s)	inside rSNPs	diseases
6	nsv470561	chr3:50158774-50584999	Flanking Active TSS Enhancers Weak transcription Genic enhancers Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	99 gene(s)	inside rSNPs	diseases
7	nsv876770	chr3:50158774-50609624	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	103 gene(s)	inside rSNPs	diseases
8	nsv1001993	chr3:50187646-50640808	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	104 gene(s)	inside rSNPs	diseases
9	esv2757870	chr3:50198478-50371377	Genic enhancers Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	74 gene(s)	inside rSNPs	diseases
10	esv2759148	chr3:50198478-50371377	Enhancers Weak transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	74 gene(s)	inside rSNPs	diseases
11	nsv834692	chr3:50198485-50393464	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	94 gene(s)	inside rSNPs	diseases
12	nsv590254	chr3:50243510-50388607	Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	93 gene(s)	inside rSNPs	diseases
13	nsv460531	chr3:50247824-50436827	Strong transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	93 gene(s)	inside rSNPs	diseases
14	nsv590255	chr3:50247824-50436827	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	93 gene(s)	inside rSNPs	diseases
15	nsv876772	chr3:50255305-50436827	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	93 gene(s)	inside rSNPs	diseases
16	nsv590257	chr3:50302830-50393640	Genic enhancers Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
17	nsv590256	chr3:50302830-50420554	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	83 gene(s)	inside rSNPs	diseases
18	nsv876774	chr3:50302830-50436827	Enhancers Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	83 gene(s)	inside rSNPs	diseases
19	nsv876773	chr3:50302830-50480131	Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
20	nsv834693	chr3:50302830-50507964	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
21	nsv876775	chr3:50324672-50504896	Flanking Active TSS Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	82 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:50357600-50358600	Flanking Active TSS	Primary hematopoietic stem cells	blood
2	chr3:50357600-50358600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr3:50357800-50358600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
4	chr3:50357800-50358600	Flanking Active TSS	Primary T cells fromperipheralblood	blood
5	chr3:50357800-50358600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr3:50357800-50358800	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
7	chr3:50357800-50360200	Active TSS	iPS-18 Cell Line	embryonic stem cell
8	chr3:50357800-50360200	Active TSS	Fetal Kidney	kidney
9	chr3:50357800-50360200	Active TSS	Pancreatic Islets	Pancreatic Islet
10	chr3:50357800-50360400	Active TSS	H9 Cell Line	embryonic stem cell
11	chr3:50357800-50360400	Active TSS	iPS-15b Cell Line	embryonic stem cell
12	chr3:50357800-50360400	Active TSS	iPS-20b Cell Line	embryonic stem cell
13	chr3:50358000-50358600	Flanking Active TSS	Primary B cells from cord blood	blood
14	chr3:50358000-50358600	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
15	chr3:50358000-50359200	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
16	chr3:50358000-50359400	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr3:50358000-50359400	Active TSS	A549	lung
18	chr3:50358000-50359400	Active TSS	HSMMtube	muscle
19	chr3:50358000-50359600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr3:50358000-50359600	Active TSS	Aorta	Aorta
21	chr3:50358000-50359600	Active TSS	Left Ventricle	heart
22	chr3:50358000-50359600	Active TSS	Small Intestine	intestine
23	chr3:50358000-50359800	Active TSS	Gastric	stomach
24	chr3:50358000-50359800	Active TSS	Right Atrium	heart
25	chr3:50358000-50360200	Active TSS	HUES48 Cell Line	embryonic stem cell
26	chr3:50358000-50360400	Active TSS	ES-I3 Cell Line	embryonic stem cell
27	chr3:50358000-50360400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
28	chr3:50358000-50360400	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr3:50358000-50360400	Active TSS	Psoas Muscle	Psoas
30	chr3:50358200-50359000	Active TSS	Cortex derived primary cultured neurospheres	brain
31	chr3:50358200-50359200	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr3:50358200-50359200	Active TSS	Fetal Muscle Trunk	muscle
33	chr3:50358200-50359200	Active TSS	Fetal Stomach	stomach
34	chr3:50358200-50359200	Active TSS	Pancreas	Pancrea
35	chr3:50358200-50359200	Active TSS	Stomach Mucosa	stomach
36	chr3:50358200-50359200	Active TSS	HMEC	breast
37	chr3:50358200-50359400	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr3:50358200-50359400	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr3:50358200-50359400	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr3:50358200-50359400	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr3:50358200-50359400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr3:50358200-50359400	Active TSS	Breast Myoepithelial Primary Cells	Breast
43	chr3:50358200-50359400	Active TSS	Primary T helper naive cells from peripheral blood	blood
44	chr3:50358200-50359400	Active TSS	Muscle Satellite Cultured Cells	--
45	chr3:50358200-50359400	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr3:50358200-50359400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr3:50358200-50359400	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr3:50358200-50359400	Active TSS	Brain Germinal Matrix	brain
49	chr3:50358200-50359400	Active TSS	Brain Hippocampus Middle	brain
50	chr3:50358200-50359400	Active TSS	Brain Inferior Temporal Lobe	brain

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