Variant report

Variant	rs11977913
Chromosome Location	chr7:150778181-150778182
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:296)
CpG islands
(count:61)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:296 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	JUND	chr7:150777156-150778283	K562	blood:	n/a	chr7:150778131-150778140
2	MYBL2	chr7:150777634-150778222	HepG2	liver:	n/a	n/a
3	REST	chr7:150777672-150778213	SK-N-SH	brain:	n/a	chr7:150778091-150778104
4	SIN3AK20	chr7:150777932-150778184	A549	lung:	n/a	n/a
5	TAF1	chr7:150777165-150779381	K562	blood:	n/a	n/a
6	POLR2A	chr7:150777141-150778793	MCF10A-Er-Src	breast:	n/a	n/a
7	SMC3	chr7:150777691-150778231	Hela-S3	cervix:	n/a	n/a
8	EP300	chr7:150777407-150778348	SK-N-SH	brain:	n/a	chr7:150778004-150778020
9	POLR2A	chr7:150777077-150778306	HepG2	liver:	n/a	n/a
10	RFX5	chr7:150777733-150778212	Hela-S3	cervix:	n/a	n/a
11	POLR2A	chr7:150770896-150778995	PANC-1	pancreas:	n/a	n/a
12	TCF12	chr7:150777330-150778328	ECC-1	luminal epithelium:	n/a	n/a
13	POLR2A	chr7:150777421-150778279	GM19099	blood:	n/a	n/a
14	TAF1	chr7:150777632-150778227	Hela-S3	cervix:	n/a	n/a
15	ZC3H11A	chr7:150777282-150778267	K562	blood:	n/a	n/a
16	POLR2A	chr7:150777491-150778342	MCF-7	breast:	n/a	n/a
17	POLR2A	chr7:150771355-150780971	HepG2	liver:	n/a	n/a
18	GABPA	chr7:150777917-150778705	H1-hESC	embryonic stem cell:	n/a	chr7:150778130-150778139 chr7:150777982-150777991
19	MAX	chr7:150777171-150778306	SK-N-SH	brain:	n/a	chr7:150778013-150778023
20	NFIC	chr7:150777711-150778277	ECC-1	luminal epithelium:	n/a	n/a
21	YY1	chr7:150777135-150778189	SK-N-SH	brain:	n/a	chr7:150778010-150778024 chr7:150777974-150777988 chr7:150777866-150777886 chr7:150777868-150777880
22	POLR2A	chr7:150777541-150778310	HUVEC	blood vessel:	n/a	n/a
23	MYBL2	chr7:150777573-150778296	HepG2	liver:	n/a	n/a
24	UBTF	chr7:150777304-150779748	K562	blood:	n/a	n/a
25	BRCA1	chr7:150777801-150778182	Hela-S3	cervix:	n/a	n/a
26	SIN3A	chr7:150777118-150778643	H1-hESC	embryonic stem cell:	n/a	n/a
27	TAF1	chr7:150777570-150778626	K562	blood:	n/a	n/a
28	E2F6	chr7:150777236-150780026	K562	blood:	n/a	chr7:150777982-150777991 chr7:150778035-150778042 chr7:150778130-150778139
29	KAP1	chr7:150777472-150778486	K562	blood:	n/a	n/a
30	PML	chr7:150776986-150778733	K562	blood:	n/a	n/a
31	MAX	chr7:150777349-150778388	A549	lung:	n/a	chr7:150778013-150778023
32	ZNF143	chr7:150777629-150778203	K562	blood:	n/a	n/a
33	ELF1	chr7:150777589-150778776	K562	blood:	n/a	chr7:150778010-150778022
34	RCOR1	chr7:150777478-150778695	K562	blood:	n/a	n/a
35	GTF2F1	chr7:150777855-150778239	Hela-S3	cervix:	n/a	n/a
36	TAF7	chr7:150777613-150778218	H1-hESC	embryonic stem cell:	n/a	n/a
37	ZBTB33	chr7:150777669-150778214	HCT-116	colon:	n/a	n/a
38	POLR2A	chr7:150777596-150778270	HCT-116	colon:	n/a	n/a
39	E2F4	chr7:150777288-150778610	K562	blood:	n/a	chr7:150777987-150777998 chr7:150777982-150777991 chr7:150778035-150778042 chr7:150778130-150778139
40	TBP	chr7:150777691-150778231	Hela-S3	cervix:	n/a	n/a
41	YY1	chr7:150777056-150778802	K562	blood:	n/a	chr7:150778010-150778024 chr7:150777974-150777988 chr7:150777866-150777886 chr7:150777868-150777880
42	POLR2A	chr7:150777637-150778223	HepG2	liver:	n/a	n/a
43	POLR2A	chr7:150777735-150778252	H1-hESC	embryonic stem cell:	n/a	n/a
44	POLR2A	chr7:150770802-150778585	Hela-S3	cervix:	n/a	n/a
45	POLR2A	chr7:150777525-150778362	K562	blood:	n/a	n/a
46	POLR2A	chr7:150777066-150779047	ECC-1	luminal epithelium:	n/a	n/a
47	YY1	chr7:150777114-150778456	SK-N-SH	brain:	n/a	chr7:150778010-150778024 chr7:150777974-150777988 chr7:150777866-150777886 chr7:150777868-150777880
48	MAX	chr7:150777131-150778415	ECC-1	luminal epithelium:	n/a	chr7:150778013-150778023
49	POLR2A	chr7:150777686-150778307	A549	lung:	n/a	n/a
50	CHD2	chr7:150777085-150778346	K562	blood:	n/a	chr7:150778118-150778128 chr7:150778128-150778138

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:150778137-150778187	HNPCEpiC	eye:	n/a
2	chr7:150778137-150778187	HRE	kidney:	n/a
3	chr7:150778137-150778187	Jurkat	blood:	n/a
4	chr7:150778137-150778187	HPAEpiC	pulmonary alveolar:	n/a
5	chr7:150778137-150778187	SK-N-SH_RA	brain:	n/a
6	chr7:150778137-150778187	T-47D	breast:	n/a
7	chr7:150778137-150778187	ECC-1	luminal epithelium:	n/a
8	chr7:150778137-150778187	SAEC	small airway:	n/a
9	chr7:150778137-150778187	MCF10A-Er-Src	breast:	n/a
10	chr7:150778137-150778187	HCPEpiC	choroid plexus:	n/a
11	chr7:150778137-150778187	SK-N-MC	brain:	n/a
12	chr7:150778137-150778187	AG09319	gingival:	n/a
13	chr7:150778137-150778187	ProgFib	skin:	n/a
14	chr7:150778137-150778187	HL-60	blood:	n/a
15	chr7:150778137-150778187	IMR90	lung:	fetal
16	chr7:150778137-150778187	HIPEpiC	eye:	n/a
17	chr7:150778137-150778187	HCM	heart:	n/a
18	chr7:150778137-150778187	BE2_C	brain:	n/a
19	chr7:150778137-150778187	GM19239	blood:	n/a
20	chr7:150778137-150778187	NB4	blood:	n/a
21	chr7:150778137-150778187	K562	blood:	n/a
22	chr7:150778137-150778187	A549	lung:	n/a
23	chr7:150778137-150778187	HRCEpiC	kidney:	n/a
24	chr7:150778137-150778187	NHDF-neo	bronchial:	n/a
25	chr7:150778137-150778187	SK-N-SH	brain:	n/a
26	chr7:150778137-150778187	ovcar-3	ovarian:	n/a
27	chr7:150778137-150778187	SKMC	muscle:	n/a
28	chr7:150778137-150778187	AG04449	skin:	fetal
29	chr7:150778137-150778187	PANC-1	pancreas:	n/a
30	chr7:150778137-150778187	MCF-7	breast:	n/a
31	chr7:150778137-150778187	CMK	blood:	n/a
32	chr7:150778137-150778187	HUVEC	blood vessel:	n/a
33	chr7:150778137-150778187	Caco-2	colon:	n/a
34	chr7:150778137-150778187	Hela-S3	cervix:	n/a
35	chr7:150778137-150778187	HAEpiC	amniotic membrane:	n/a
36	chr7:150778137-150778187	NHBE	bronchial:	n/a
37	chr7:150778137-150778187	PFSK-1	brain:	n/a
38	chr7:150778137-150778187	GM12891	blood:	n/a
39	chr7:150778137-150778187	HRPEpiC	eye:	n/a
40	chr7:150778137-150778187	HepG2	liver:	n/a
41	chr7:150778137-150778187	AG10803	skin:	n/a
42	chr7:150778137-150778187	U87	brain:	n/a
43	chr7:150778137-150778187	AG04450	lung:	fetal
44	chr7:150778137-150778187	H1-hESC	embryonic stem cell:	embryo
45	chr7:150778137-150778187	AoSMC	blood vessel:	n/a
46	chr7:150778137-150778187	PrEC	prostate:	n/a
47	chr7:150778137-150778187	RPTEC	kidney:	n/a
48	chr7:150778137-150778187	GM06990	blood:	n/a
49	chr7:150778137-150778187	HMEC	breast:	n/a
50	chr7:150778137-150778187	HCF	heart:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:5568664..5571530-chr7:150777332..150779644,2	MCF-7	breast:
2	chr7:150776319..150779502-chr7:150929825..150933736,3	K562	blood:
3	chr17:7387035..7388026-chr7:150777937..150778541,2	Hela-S3	cervix:
4	chr3:195808539..195809040-chr7:150777822..150778322,2	Hela-S3	cervix:
5	chr7:149468652..149471157-chr7:150776207..150778297,2	MCF-7	breast:
6	chr1:245133109..245133735-chr7:150778030..150778899,2	Hela-S3	cervix:
7	chr2:200322138..200322776-chr7:150777864..150778406,2	NB4	blood:

No data

Variant related genes	Relation type
ENSG00000244151	TF binding region
AGAP3	TF binding region
FASTK	TF binding region
FASTK	CpG island
ENSG00000244151	CpG island
AGAP3	CpG island
ENSG00000181444	Chromatin interaction
ENSG00000075624	Chromatin interaction
ENSG00000119042	Chromatin interaction
ENSG00000174282	Chromatin interaction
ENSG00000072274	Chromatin interaction
ENSG00000203666	Chromatin interaction
ENSG00000033100	Chromatin interaction
ENSG00000181222	Chromatin interaction
ENSG00000225953	Chromatin interaction

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs11973649	1.00[ASW][hapmap]
rs11976118	1.00[ASN][1000 genomes]
rs11979696	1.00[AMR][1000 genomes]
rs11983213	1.00[ASW][hapmap];1.00[MKK][hapmap];1.00[AMR][1000 genomes]
rs11983731	1.00[AMR][1000 genomes]
rs2069446	1.00[AMR][1000 genomes]
rs2069457	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];0.85[YRI][hapmap]
rs34058458	1.00[MEX][hapmap]
rs34158168	1.00[AMR][1000 genomes]
rs3918158	1.00[LWK][hapmap];1.00[MKK][hapmap]
rs3918159	1.00[LWK][hapmap];1.00[MKK][hapmap]
rs3918198	1.00[AMR][1000 genomes]
rs3918211	1.00[ASN][1000 genomes]
rs3918235	1.00[EUR][1000 genomes]
rs61652080	1.00[AMR][1000 genomes]
rs73472561	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73474675	1.00[ASN][1000 genomes]
rs7776461	1.00[AMR][1000 genomes]
rs7776772	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:26 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1821419	chr7:150593315-150974269	Enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	128 gene(s)	inside rSNPs	diseases
2	nsv1022246	chr7:150619660-150779924	Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Genic enhancers Enhancers Weak transcription Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
3	nsv889465	chr7:150640285-150800823	Flanking Active TSS Strong transcription Enhancers Flanking Bivalent TSS/Enh Genic enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
4	nsv1017863	chr7:150643928-150779924	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	52 gene(s)	inside rSNPs	diseases
5	nsv539197	chr7:150643928-150779924	Bivalent/Poised TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	52 gene(s)	inside rSNPs	diseases
6	nsv1028645	chr7:150643928-150806534	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Active TSS Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	59 gene(s)	inside rSNPs	diseases
7	nsv539198	chr7:150643928-150879259	Weak transcription Enhancers Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	72 gene(s)	inside rSNPs	diseases
8	nsv889476	chr7:150729212-150951819	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Bivalent Enhancer 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	120 gene(s)	inside rSNPs	diseases
9	nsv1031733	chr7:150730999-150790517	Transcr. at gene 5' and 3' Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	47 gene(s)	inside rSNPs	diseases
10	nsv889477	chr7:150731698-150837529	Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Strong transcription Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	57 gene(s)	inside rSNPs	diseases
11	nsv889478	chr7:150732812-150889527	Strong transcription Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	61 gene(s)	inside rSNPs	diseases
12	nsv831188	chr7:150735204-150912875	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Bivalent/Poised TSS Genic enhancers 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 target site	64 gene(s)	inside rSNPs	diseases
13	nsv889479	chr7:150736382-150785321	Flanking Active TSS Active TSS Enhancers Genic enhancers Bivalent Enhancer Weak transcription Strong transcription 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	45 gene(s)	inside rSNPs	diseases
14	nsv889480	chr7:150736382-150797581	Active TSS Bivalent Enhancer Genic enhancers Flanking Active TSS Strong transcription Enhancers Weak transcription 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	46 gene(s)	inside rSNPs	diseases
15	nsv1028023	chr7:150738624-150790517	Strong transcription Genic enhancers Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	44 gene(s)	inside rSNPs	diseases
16	nsv465214	chr7:150751590-150822192	Flanking Active TSS Enhancers Bivalent/Poised TSS Genic enhancers Strong transcription Weak transcription Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	52 gene(s)	inside rSNPs	diseases
17	nsv609012	chr7:150751590-150822192	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Strong transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	52 gene(s)	inside rSNPs	diseases
18	nsv609013	chr7:150751590-150832913	Active TSS Strong transcription Flanking Active TSS Bivalent/Poised TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	52 gene(s)	inside rSNPs	diseases
19	nsv465215	chr7:150762871-150825087	Enhancers Strong transcription Weak transcription Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
20	nsv609014	chr7:150762871-150825087	Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
21	nsv889481	chr7:150766799-150837529	Weak transcription Genic enhancers Flanking Active TSS Active TSS Strong transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
22	nsv889482	chr7:150766799-150851566	Genic enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Enhancers Weak transcription Active TSS 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	45 gene(s)	inside rSNPs	diseases
23	nsv889483	chr7:150773165-150787046	Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	26 gene(s)	inside rSNPs	diseases
24	nsv889484	chr7:150774308-150787046	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Weak transcription Enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	26 gene(s)	inside rSNPs	diseases
25	nsv889485	chr7:150774308-150788304	Strong transcription Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	27 gene(s)	inside rSNPs	diseases
26	nsv889486	chr7:150775306-150891641	Enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	48 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	chr7:150776200-150779400	Transcr. at gene 5' and 3'	Dnd41	blood
2	chr7:150776400-150778600	Active TSS	HUES48 Cell Line	embryonic stem cell
3	chr7:150776400-150780000	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
4	chr7:150776600-150778400	Flanking Active TSS	Primary hematopoietic stem cells	blood
5	chr7:150776600-150778800	Active TSS	iPS-15b Cell Line	embryonic stem cell
6	chr7:150776800-150781000	Active TSS	H9 Cell Line	embryonic stem cell
7	chr7:150776800-150781200	Active TSS	Pancreatic Islets	Pancreatic Islet
8	chr7:150777000-150778200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr7:150777000-150778200	Flanking Active TSS	Primary B cells from cord blood	blood
10	chr7:150777000-150778200	Active TSS	Sigmoid Colon	Sigmoid Colon
11	chr7:150777000-150778400	Active TSS	ES-I3 Cell Line	embryonic stem cell
12	chr7:150777000-150778400	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr7:150777000-150778400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr7:150777000-150778400	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
15	chr7:150777000-150778400	Active TSS	Fetal Kidney	kidney
16	chr7:150777000-150778600	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr7:150777000-150778600	Active TSS	Ovary	ovary
18	chr7:150777000-150778600	Active TSS	Placenta Amnion	Placenta Amnion
19	chr7:150777000-150778600	Active TSS	A549	lung
20	chr7:150777000-150778800	Active TSS	Right Atrium	heart
21	chr7:150777000-150781000	Active TSS	iPS-20b Cell Line	embryonic stem cell
22	chr7:150777200-150778200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr7:150777200-150778200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr7:150777200-150778200	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
25	chr7:150777200-150778200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr7:150777200-150778200	Active TSS	Duodenum Smooth Muscle	Duodenum
27	chr7:150777200-150778200	Active TSS	Fetal Intestine Large	intestine
28	chr7:150777200-150778200	Active TSS	Fetal Lung	lung
29	chr7:150777200-150778200	Active TSS	Fetal Stomach	stomach
30	chr7:150777200-150778200	Active TSS	Thymus	Thymus
31	chr7:150777200-150778200	Active TSS	GM12878-XiMat	blood
32	chr7:150777200-150778200	Active TSS	Hela-S3	cervix
33	chr7:150777200-150778200	Active TSS	NHLF	lung
34	chr7:150777200-150778400	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr7:150777200-150778400	Active TSS	Aorta	Aorta
36	chr7:150777200-150778600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr7:150777200-150778600	Active TSS	Colon Smooth Muscle	Colon
38	chr7:150777200-150778600	Active TSS	Esophagus	oesophagus
39	chr7:150777200-150778600	Active TSS	Fetal Intestine Small	intestine
40	chr7:150777200-150778600	Active TSS	Left Ventricle	heart
41	chr7:150777200-150778800	Active TSS	HUES6 Cell Line	embryonic stem cell
42	chr7:150777200-150778800	Active TSS	HUES64 Cell Line	embryonic stem cell
43	chr7:150777200-150778800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr7:150777200-150778800	Active TSS	HSMM	muscle
45	chr7:150777200-150779000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
46	chr7:150777200-150780600	Active TSS	Small Intestine	intestine
47	chr7:150777200-150780800	Active TSS	iPS-18 Cell Line	embryonic stem cell
48	chr7:150777400-150778200	Active TSS	Primary T cells from cord blood	blood
49	chr7:150777400-150778200	Active TSS	Brain Germinal Matrix	brain
50	chr7:150777400-150778200	Active TSS	Brain Substantia Nigra	brain

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