Variant report

Variant	rs1076872
Chromosome Location	chr3:50329826-50329827
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:451)
CpG islands
(count:0)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:451 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr3:50329736-50330247	K562	blood:	n/a	n/a
2	GABPA	chr3:50329756-50330129	A549	lung:	n/a	n/a
3	STAT1	chr3:50329755-50330279	GM12878	blood:	n/a	n/a
4	TAF1	chr3:50329633-50330056	PFSK-1	brain:	n/a	n/a
5	RUNX3	chr3:50329623-50330395	GM12878	blood:	n/a	n/a
6	ZBTB33	chr3:50329673-50330067	A549	lung:	n/a	n/a
7	POU2F2	chr3:50329607-50330107	GM12891	blood:	n/a	n/a
8	POLR2A	chr3:50329565-50330436	HL-60	blood:	n/a	n/a
9	MAX	chr3:50329052-50330304	H1-hESC	embryonic stem cell:	n/a	chr3:50329496-50329507 chr3:50329599-50329609
10	ELK1	chr3:50329775-50330253	Hela-S3	cervix:	n/a	n/a
11	RUNX3	chr3:50329608-50330410	GM12878	blood:	n/a	n/a
12	POLR2A	chr3:50329614-50330336	HUVEC	blood vessel:	n/a	n/a
13	NFYA	chr3:50329768-50330126	Hela-S3	cervix:	n/a	n/a
14	TCF7L2	chr3:50329791-50330024	Hela-S3	cervix:	n/a	n/a
15	TAF1	chr3:50329555-50330271	GM12878	blood:	n/a	n/a
16	POLR2A	chr3:50329636-50329889	GM12891	blood:	n/a	n/a
17	TBP	chr3:50329634-50330298	K562	blood:	n/a	n/a
18	ATF2	chr3:50329646-50330216	GM12878	blood:	n/a	n/a
19	PML	chr3:50328914-50330626	GM12878	blood:	n/a	n/a
20	POU2F2	chr3:50329693-50330092	GM12878	blood:	n/a	n/a
21	BRCA1	chr3:50329794-50330282	HepG2	liver:	n/a	n/a
22	MAX	chr3:50329167-50330342	H1-hESC	embryonic stem cell:	n/a	chr3:50329496-50329507 chr3:50329599-50329609
23	HEY1	chr3:50329521-50330376	HepG2	liver:	n/a	n/a
24	CBX3	chr3:50329663-50330222	K562	blood:	n/a	n/a
25	MAX	chr3:50328952-50330655	HCT-116	colon:	n/a	chr3:50329496-50329507 chr3:50329599-50329609
26	YY1	chr3:50329563-50330175	GM12891	blood:	n/a	chr3:50329601-50329612
27	NR2F2	chr3:50329192-50330300	K562	blood:	n/a	n/a
28	NANOG	chr3:50329772-50330252	H1-hESC	embryonic stem cell:	n/a	n/a
29	YY1	chr3:50329587-50330198	H1-hESC	embryonic stem cell:	n/a	chr3:50329601-50329612
30	CEBPD	chr3:50329687-50330299	K562	blood:	n/a	n/a
31	HEY1	chr3:50329610-50330327	K562	blood:	n/a	n/a
32	RCOR1	chr3:50329799-50330294	K562	blood:	n/a	n/a
33	POLR2A	chr3:50329500-50330375	ECC-1	luminal epithelium:	n/a	n/a
34	POLR2A	chr3:50329642-50330365	GM12891	blood:	n/a	n/a
35	RELA	chr3:50329405-50330328	GM15510	blood:	n/a	n/a
36	MAX	chr3:50329293-50330249	K562	blood:	n/a	chr3:50329496-50329507 chr3:50329599-50329609
37	MAX	chr3:50328956-50330343	ECC-1	luminal epithelium:	n/a	chr3:50329496-50329507 chr3:50329599-50329609
38	ZNF263	chr3:50329756-50330942	HEK293-T-REx	kidney:	n/a	n/a
39	MAX	chr3:50329038-50330300	A549	lung:	n/a	chr3:50329496-50329507 chr3:50329599-50329609
40	TAF1	chr3:50329667-50329924	GM12891	blood:	n/a	n/a
41	E2F6	chr3:50329062-50330373	H1-hESC	embryonic stem cell:	n/a	chr3:50329600-50329609 chr3:50329626-50329635
42	YY1	chr3:50329648-50330200	H1-hESC	embryonic stem cell:	n/a	n/a
43	POLR2A	chr3:50329071-50330804	U87	brain:	n/a	n/a
44	USF2	chr3:50329807-50330509	Hela-S3	cervix:	n/a	n/a
45	POLR2A	chr3:50329529-50330447	GM12891	blood:	n/a	n/a
46	MAX	chr3:50328984-50330280	K562	blood:	n/a	chr3:50329496-50329507 chr3:50329599-50329609
47	SMARCC2	chr3:50329775-50330311	Hela-S3	cervix:	n/a	n/a
48	POLR2A	chr3:50329631-50330326	GM12892	blood:	n/a	n/a
49	FOXA2	chr3:50329732-50330066	A549	lung:	n/a	n/a
50	STAT5A	chr3:50329719-50330185	K562	blood:	n/a	chr3:50329871-50329895

No data

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:50329739..50332601-chr3:50372246..50375675,3	MCF-7	breast:
2	chr3:50272542..50276085-chr3:50328223..50330525,3	MCF-7	breast:
3	chr3:50263469..50266686-chr3:50327913..50330648,3	MCF-7	breast:
4	chr3:50296030..50318456-chr3:50318822..50339499,66	MCF-7	breast:
5	chr1:37939822..37940626-chr3:50329788..50330366,2	HCT-116	colon:
6	chr21:48054963..48055735-chr3:50329204..50329933,2	NB4	blood:
7	chr3:50328544..50331099-chr3:50341314..50343587,2	MCF-7	breast:
8	chr3:50327926..50342388-chr3:50350886..50359960,36	MCF-7	breast:
9	chr3:50273529..50275833-chr3:50328515..50330856,2	K562	blood:
10	chr3:50305234..50312110-chr3:50326257..50332221,8	MCF-7	breast:
11	chr3:50324564..50342616-chr3:50350801..50362499,49	MCF-7	breast:
12	chr3:50310426..50313247-chr3:50328333..50331056,2	K562	blood:
13	chr3:50315763..50317890-chr3:50327767..50331626,3	K562	blood:
14	chr3:50263477..50265556-chr3:50328393..50331369,3	K562	blood:
15	chr3:50325622..50330493-chr3:50373581..50377874,6	K562	blood:
16	chr3:50326497..50331702-chr3:50356299..50362839,8	K562	blood:
17	chr3:50328785..50330512-chr3:50359361..50362039,2	K562	blood:
18	chr3:50327690..50333528-chr3:50363706..50369146,7	MCF-7	breast:

No data

Variant related genes	Relation type
IFRD2	TF binding region
ENSG00000068001	Chromatin interaction
ENSG00000114353	Chromatin interaction
ENSG00000230454	Chromatin interaction
ENSG00000179564	Chromatin interaction
ENSG00000160310	Chromatin interaction
ENSG00000232352	Chromatin interaction
ENSG00000068028	Chromatin interaction
ENSG00000114378	Chromatin interaction
ENSG00000114383	Chromatin interaction
ENSG00000163874	Chromatin interaction
ENSG00000233621	Chromatin interaction
ENSG00000012171	Chromatin interaction

Extended variants
information (count: 38 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs11557220	1.00[YRI][hapmap]
rs11715758	0.82[ASN][1000 genomes]
rs11917680	0.94[CHD][hapmap];0.82[MEX][hapmap]
rs12637870	0.94[CHD][hapmap];0.83[MKK][hapmap]
rs2236989	0.94[CHD][hapmap]
rs2282755	0.94[CHD][hapmap];0.88[MEX][hapmap]
rs41499647	0.94[CHD][hapmap]
rs4547694	0.82[ASW][hapmap];0.91[CEU][hapmap];0.94[CHB][hapmap];1.00[CHD][hapmap];0.95[JPT][hapmap];0.80[TSI][hapmap];0.83[ASN][1000 genomes]
rs709210	1.00[ASW][hapmap];0.87[CHB][hapmap];1.00[CHD][hapmap]
rs9877046	1.00[ASW][hapmap];0.83[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.94[MEX][hapmap];0.91[MKK][hapmap];0.84[TSI][hapmap];0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:28 , 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	nsv1013949	chr3:50151712-50339163	Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
3	nsv590250	chr3:50153356-50332697	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
4	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
5	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
6	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
7	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
8	nsv590251	chr3:50158774-50337422	Active TSS Strong transcription Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
9	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
10	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
11	nsv523560	chr3:50172397-50339163	Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Genic enhancers Strong transcription 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	53 gene(s)	inside rSNPs	diseases
12	nsv1014256	chr3:50187646-50339163	Enhancers Active TSS Strong transcription Weak transcription Genic enhancers Bivalent/Poised TSS Flanking Active TSS 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	53 gene(s)	inside rSNPs	diseases
13	nsv536565	chr3:50187646-50339163	Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
14	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
15	nsv590253	chr3:50196418-50337422	Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
16	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
17	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
18	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
19	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
20	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
21	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
22	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
23	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
24	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
25	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
26	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
27	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
28	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

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs1076872	HYAL3	cis	Esophagus Muscularis	GTEx
rs1076872	PER3	trans	lymphoblastoid	seeQTL

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:50328200-50330200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr3:50328400-50330000	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr3:50328400-50330000	Active TSS	Hela-S3	cervix
4	chr3:50328400-50330000	Active TSS	HMEC	breast
5	chr3:50328400-50330200	Active TSS	GM12878-XiMat	blood
6	chr3:50328400-50330600	Active TSS	A549	lung
7	chr3:50328600-50330000	Active TSS	H1 Cell Line	embryonic stem cell
8	chr3:50328600-50330000	Active TSS	HUES6 Cell Line	embryonic stem cell
9	chr3:50328600-50330000	Active TSS	HSMM	muscle
10	chr3:50328600-50330000	Active TSS	NHLF	lung
11	chr3:50328600-50330200	Active TSS	HUES48 Cell Line	embryonic stem cell
12	chr3:50328600-50330200	Active TSS	iPS-20b Cell Line	embryonic stem cell
13	chr3:50328600-50330200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr3:50328600-50330200	Active TSS	Breast Myoepithelial Primary Cells	Breast
15	chr3:50328600-50330200	Active TSS	K562	blood
16	chr3:50328600-50330400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr3:50328600-50330400	Active TSS	Small Intestine	intestine
18	chr3:50328600-50330600	Active TSS	HUES64 Cell Line	embryonic stem cell
19	chr3:50328800-50330000	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr3:50328800-50330200	Active TSS	ES-I3 Cell Line	embryonic stem cell
21	chr3:50328800-50330200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr3:50328800-50330200	Active TSS	H9 Cell Line	embryonic stem cell
23	chr3:50328800-50330200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr3:50328800-50330200	Active TSS	iPS-15b Cell Line	embryonic stem cell
25	chr3:50328800-50330200	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr3:50328800-50330200	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr3:50328800-50330200	Active TSS	Fetal Kidney	kidney
28	chr3:50328800-50330200	Active TSS	Gastric	stomach
29	chr3:50328800-50330200	Active TSS	Sigmoid Colon	Sigmoid Colon
30	chr3:50328800-50330200	Active TSS	HSMMtube	muscle
31	chr3:50328800-50330200	Active TSS	NHDF-Ad	bronchial
32	chr3:50328800-50330400	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr3:50328800-50330400	Active TSS	Pancreatic Islets	Pancreatic Islet
34	chr3:50329000-50330000	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr3:50329000-50330000	Active TSS	Muscle Satellite Cultured Cells	--
36	chr3:50329000-50330000	Active TSS	Lung	lung
37	chr3:50329000-50330000	Active TSS	NHEK	skin
38	chr3:50329000-50330200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr3:50329000-50330200	Active TSS	iPS-18 Cell Line	embryonic stem cell
40	chr3:50329000-50330200	Active TSS	Primary T helper cells PMA-I stimulated	--
41	chr3:50329000-50330200	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr3:50329000-50330200	Active TSS	Left Ventricle	heart
43	chr3:50329000-50330200	Active TSS	Ovary	ovary
44	chr3:50329000-50330200	Active TSS	Right Ventricle	heart
45	chr3:50329000-50330200	Bivalent/Poised TSS	HepG2	liver
46	chr3:50329000-50330600	Active TSS	Psoas Muscle	Psoas
47	chr3:50329200-50330000	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr3:50329200-50330000	Active TSS	Liver	Liver
49	chr3:50329200-50330000	Active TSS	Fetal Lung	lung
50	chr3:50329200-50330000	Active TSS	Placenta Amnion	Placenta Amnion

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