Variant report

Variant	rs1962004
Chromosome Location	chr7:150020381-150020382
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:356)
CpG islands
(count:0)
Chromatin interactive
region (count:19)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:356 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	TEAD4	chr7:150019027-150021103	K562	blood:	n/a	n/a
2	STAT5A	chr7:150019649-150020426	GM12878	blood:	n/a	n/a
3	SMARCA4	chr7:150019611-150021724	K562	blood:	n/a	n/a
4	CTCF	chr7:150020328-150020685	H1-hESC	embryonic stem cell:	n/a	n/a
5	TAF1	chr7:150019902-150020448	GM12892	blood:	n/a	n/a
6	TBL1XR1	chr7:150019978-150021092	GM12878	blood:	n/a	n/a
7	ELF1	chr7:150020005-150020837	HepG2	liver:	n/a	n/a
8	NRF1	chr7:150020124-150020575	SK-N-SH	brain:	n/a	chr7:150020276-150020287
9	POLR2A	chr7:150019063-150020988	K562	blood:	n/a	n/a
10	SREBP1	chr7:150019233-150021870	GM12878	blood:	n/a	n/a
11	POLR2A	chr7:150019834-150021064	GM12878	blood:	n/a	n/a
12	JUND	chr7:150020167-150020940	HepG2	liver:	n/a	n/a
13	E2F6	chr7:150019828-150021009	K562	blood:	n/a	n/a
14	POLR2A	chr7:150019076-150021113	HepG2	liver:	n/a	n/a
15	MYC	chr7:150019334-150021318	K562	blood:	n/a	n/a
16	POLR2A	chr7:150019965-150020679	HepG2	liver:	n/a	n/a
17	TBP	chr7:150020017-150020938	HepG2	liver:	n/a	n/a
18	TBL1XR1	chr7:150019513-150020430	K562	blood:	n/a	n/a
19	MYBL2	chr7:150019745-150020968	HepG2	liver:	n/a	n/a
20	ZBTB7A	chr7:150019984-150020944	ECC-1	luminal epithelium:	n/a	n/a
21	MYC	chr7:150019358-150021028	K562	blood:	n/a	n/a
22	POLR2A	chr7:150018810-150021240	GM12892	blood:	n/a	n/a
23	SMC3	chr7:150020047-150021957	Hela-S3	cervix:	n/a	n/a
24	ELF1	chr7:150019901-150020923	GM12878	blood:	n/a	n/a
25	MAX	chr7:150019757-150021042	K562	blood:	n/a	n/a
26	MYC	chr7:150019424-150021111	K562	blood:	n/a	n/a
27	BCLAF1	chr7:150019870-150020627	GM12878	blood:	n/a	n/a
28	TBL1XR1	chr7:150019299-150021577	K562	blood:	n/a	n/a
29	REST	chr7:150020320-150021091	K562	blood:	n/a	n/a
30	RAD21	chr7:150020375-150020836	K562	blood:	n/a	n/a
31	POLR2A	chr7:150019955-150020838	HCT-116	colon:	n/a	n/a
32	POLR2A	chr7:150018930-150021583	GM12878	blood:	n/a	n/a
33	EGR1	chr7:150020089-150020783	K562	blood:	n/a	n/a
34	POLR2A	chr7:150019855-150020970	HCT-116	colon:	n/a	n/a
35	YY1	chr7:150019092-150021130	GM12878	blood:	n/a	n/a
36	POLR2A	chr7:150019991-150020744	HepG2	liver:	n/a	n/a
37	JUN	chr7:150019613-150020540	K562	blood:	n/a	n/a
38	MXI1	chr7:150019817-150021362	Hela-S3	cervix:	n/a	n/a
39	POLR2A	chr7:150019994-150020992	GM10847	blood:	n/a	n/a
40	MBD4	chr7:150019712-150020511	HepG2	liver:	n/a	n/a
41	HDAC2	chr7:150019902-150020813	HepG2	liver:	n/a	n/a
42	BCLAF1	chr7:150019882-150021218	GM12878	blood:	n/a	n/a
43	GABPA	chr7:150020072-150020784	H1-hESC	embryonic stem cell:	n/a	n/a
44	NFATC1	chr7:150019480-150020630	GM12878	blood:	n/a	n/a
45	CCNT2	chr7:150019894-150020892	K562	blood:	n/a	n/a
46	SP1	chr7:150019977-150020530	GM12878	blood:	n/a	n/a
47	JUND	chr7:150020014-150020534	HepG2	liver:	n/a	n/a
48	POLR2A	chr7:150019461-150021081	GM18951	blood:	n/a	n/a
49	POLR2A	chr7:150019080-150021119	GM18526	blood:	n/a	n/a
50	POLR2A	chr7:150019842-150020540	PANC-1	pancreas:	n/a	n/a

No data

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:150019150..150025305-chr7:150035524..150043799,10	MCF-7	breast:
2	chr7:150018389..150025798-chr7:150030734..150040389,17	MCF-7	breast:
3	chr7:150019286..150021465-chr7:150069323..150073240,4	MCF-7	breast:
4	chr7:150019550..150021994-chr7:150069161..150070677,2	K562	blood:
5	chr7:150017186..150022010-chr7:150063447..150067622,10	K562	blood:
6	chr7:150016171..150021897-chr7:150062899..150068795,19	MCF-7	breast:
7	chr7:150017073..150026383-chr7:150074145..150079980,13	MCF-7	breast:
8	chr4:87926172..87928696-chr7:150019642..150022141,2	MCF-7	breast:
9	chr7:148822477..148824067-chr7:150018763..150021367,2	MCF-7	breast:
10	chr7:150018966..150021782-chr7:150094675..150098930,7	K562	blood:
11	chr7:150018539..150023441-chr7:150073756..150077036,7	MCF-7	breast:
12	chr7:150017344..150021301-chr7:150099535..150103707,10	K562	blood:
13	chr7:150020223..150020755-chr7:150064934..150065818,2	Hela-S3	cervix:
14	chr7:150019910..150022890-chr7:150026315..150029098,3	MCF-7	breast:
15	chr7:150018857..150021301-chr7:150100532..150103886,6	K562	blood:
16	chr7:150018458..150023402-chr7:150064103..150067772,7	MCF-7	breast:
17	chr7:150019591..150022356-chr7:150674947..150677441,2	K562	blood:
18	chr7:150017186..150022141-chr7:150063447..150068849,12	K562	blood:
19	chr7:150018966..150021939-chr7:150095611..150098750,5	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LRRC61-3	chr7:150020305-150020649	NONHSAT124103

No data

Variant related genes	Relation type
ACTR3C	TF binding region
ENSG00000055118	Chromatin interaction
ENSG00000197024	Chromatin interaction
ENSG00000106538	Chromatin interaction
ENSG00000261305	Chromatin interaction
ENSG00000240449	Chromatin interaction
ENSG00000196456	Chromatin interaction
ENSG00000214022	Chromatin interaction
ENSG00000204947	Chromatin interaction
ENSG00000188707	Chromatin interaction
ENSG00000240877	Chromatin interaction
ENSG00000172493	Chromatin interaction

Extended variants
information (count: 86 )
Associated
traits (count: 20 )

rSNPs within LD-proxies of this variant (count:71)

rs_ID	r²[population]
rs10282458	0.82[EUR][1000 genomes]
rs1047207	0.89[EUR][1000 genomes]
rs1047575	0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1047586	0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10952249	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10952250	0.86[CEU][hapmap];0.88[EUR][1000 genomes]
rs10952252	0.82[EUR][1000 genomes]
rs11764936	0.86[CEU][hapmap];0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11765644	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11765692	0.89[EUR][1000 genomes]
rs11766288	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11767726	1.00[CEU][hapmap];0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11769348	0.86[CEU][hapmap];0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11773351	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11974980	0.93[CEU][hapmap];0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11975886	0.93[CEU][hapmap];0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11983355	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1464752	0.86[EUR][1000 genomes]
rs1464753	0.89[EUR][1000 genomes]
rs17173617	0.89[EUR][1000 genomes]
rs17837498	1.00[CEU][hapmap];0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1916932	0.89[EUR][1000 genomes]
rs1983440	0.86[CEU][hapmap];0.89[EUR][1000 genomes]
rs2098053	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2108851	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2108852	1.00[CEU][hapmap];0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2108853	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2108854	1.00[CEU][hapmap];0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2159234	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2159235	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2159236	1.00[CEU][hapmap];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2373751	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs28432021	0.82[EUR][1000 genomes]
rs28439010	0.82[EUR][1000 genomes]
rs3088207	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs34489187	0.82[EUR][1000 genomes]
rs3735167	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs3735169	0.86[CEU][hapmap];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3735170	0.85[CEU][hapmap];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3735171	0.86[CEU][hapmap];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3735172	0.86[CEU][hapmap];0.89[EUR][1000 genomes]
rs3735173	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs3735174	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs3735175	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs3800780	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3800781	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4395803	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4554381	0.86[CEU][hapmap];0.88[EUR][1000 genomes]
rs55715989	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs55881542	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs55974958	0.89[EUR][1000 genomes]
rs56019796	0.88[EUR][1000 genomes]
rs56190213	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs56402329	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs56923535	0.88[EUR][1000 genomes]
rs56998970	0.88[EUR][1000 genomes]
rs57888387	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs59572505	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs60268791	0.88[EUR][1000 genomes]
rs60283368	0.89[EUR][1000 genomes]
rs60467296	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs61421252	0.89[EUR][1000 genomes]
rs6964110	0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs73170169	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs73170174	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs73170185	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs73170192	0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7781827	0.93[CEU][hapmap];0.88[EUR][1000 genomes]
rs7788316	0.93[CEU][hapmap];0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7806429	0.93[CEU][hapmap];0.88[EUR][1000 genomes]
rs883138	0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1034409	chr7:149844639-150447071	Flanking Active TSS Active TSS Genic enhancers Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	75 gene(s)	inside rSNPs	diseases
2	nsv608990	chr7:149961274-150707488	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
3	nsv1015582	chr7:149967986-150285104	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
4	nsv508490	chr7:150006068-150051241	Weak transcription Transcr. at gene 5' and 3' Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
5	nsv889453	chr7:150009838-150104410	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription Genic enhancers Bivalent Enhancer 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 target site	50 gene(s)	inside rSNPs	diseases
6	nsv889454	chr7:150009838-150115183	Strong transcription Flanking Active TSS Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
7	nsv889455	chr7:150013393-150104410	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
8	nsv889456	chr7:150013393-150115183	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
9	nsv1017368	chr7:150016952-150655773	Bivalent Enhancer ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription Active TSS Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
10	nsv539195	chr7:150016952-150655773	Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
11	nsv516052	chr7:150020295-150034184	Genic enhancers Strong transcription Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS 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 miRNA target site	16 gene(s)	inside rSNPs	diseases
12	nsv518774	chr7:150020295-150036664	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
13	nsv889457	chr7:150020295-150104410	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Strong transcription Bivalent Enhancer 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 target site	50 gene(s)	inside rSNPs	diseases
14	nsv889458	chr7:150020295-150115183	Enhancers Flanking Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
15	nsv521407	chr7:150020295-150118590	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh 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	50 gene(s)	inside rSNPs	diseases

mRNA abundance (count:20)

SNP	Gene	Cis/trans	Tissue	Source
rs1962004	LRRC61	cis	Skin Sun Exposed Lower leg	GTEx
rs1962004	LRRC61	cis	Nerve Tibial	GTEx
rs1962004	ZBED6CL	cis	Whole Blood	GTEx
rs1962004	LRRC61	cis	Artery Tibial	GTEx
rs1962004	ZBED6CL	cis	Esophagus Muscularis	GTEx
rs1962004	LRRC61	cis	multi-tissue	Pritchard
rs1962004	LRRC61	cis	Adipose Subcutaneous	GTEx
rs1962004	LRRC61	cis	lung	GTEx
rs1962004	ACTR3C	cis	Muscle Skeletal	GTEx
rs1962004	LRRC61	cis	Muscle Skeletal	GTEx
rs1962004	C7orf29	Cis_1M	lymphoblastoid	RTeQTL
rs1962004	LRRC61	Cis_1M	lymphoblastoid	RTeQTL
rs1962004	LRRC61	cis	Artery Aorta	GTEx
rs1962004	LRRC61	cis	Esophagus Muscularis	GTEx
rs1962004	RARRES2	cis	multi-tissue	Pritchard
rs1962004	LRRC61	cis	Esophagus Mucosa	GTEx
rs1962004	REPIN1	cis	Muscle Skeletal	GTEx
rs1962004	LRRC61	cis	Thyroid	GTEx
rs1962004	RARRES2	cis	normal skin	skin_eQTL
rs1962004	ZBED6CL	cis	lung	GTEx

Chromatin state (count:119 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:150018200-150020800	Weak transcription	HSMM	muscle
2	chr7:150018200-150021400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr7:150018800-150020800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr7:150019000-150022000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr7:150019200-150020800	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr7:150019200-150021000	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
7	chr7:150019200-150022000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr7:150019200-150022000	Active TSS	Rectal Smooth Muscle	rectum
9	chr7:150019400-150020800	Active TSS	Brain Inferior Temporal Lobe	brain
10	chr7:150019400-150021200	Active TSS	Brain Angular Gyrus	brain
11	chr7:150019400-150021200	Active TSS	Esophagus	oesophagus
12	chr7:150019400-150021400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr7:150019400-150021600	Active TSS	Brain Germinal Matrix	brain
14	chr7:150019400-150021800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
15	chr7:150019400-150021800	Active TSS	Pancreatic Islets	Pancreatic Islet
16	chr7:150019600-150020400	Flanking Active TSS	Primary B cells from peripheral blood	blood
17	chr7:150019600-150020400	Active TSS	Colonic Mucosa	Colon
18	chr7:150019600-150020400	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
19	chr7:150019600-150020400	Flanking Active TSS	Fetal Lung	lung
20	chr7:150019600-150020400	Flanking Active TSS	Fetal Thymus	thymus
21	chr7:150019600-150020400	Flanking Active TSS	NHEK	skin
22	chr7:150019600-150020600	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr7:150019600-150020800	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
24	chr7:150019600-150020800	Active TSS	Brain Hippocampus Middle	brain
25	chr7:150019600-150021000	Active TSS	HUES6 Cell Line	embryonic stem cell
26	chr7:150019600-150021000	Active TSS	Primary T killer naive cells fromperipheralblood	blood
27	chr7:150019600-150021000	Active TSS	Right Ventricle	heart
28	chr7:150019600-150021200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr7:150019600-150021200	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
30	chr7:150019600-150021200	Active TSS	Sigmoid Colon	Sigmoid Colon
31	chr7:150019600-150021400	Active TSS	H9 Cell Line	embryonic stem cell
32	chr7:150019600-150021400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr7:150019600-150021600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
34	chr7:150019600-150021800	Flanking Active TSS	Primary hematopoietic stem cells	blood
35	chr7:150019600-150022000	Flanking Active TSS	Adipose Nuclei	Adipose
36	chr7:150019600-150022000	Flanking Active TSS	Stomach Smooth Muscle	stomach
37	chr7:150019600-150022200	Flanking Active TSS	Primary B cells from cord blood	blood
38	chr7:150019800-150020400	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
39	chr7:150019800-150020400	Flanking Active TSS	Placenta	Placenta
40	chr7:150019800-150020400	Bivalent/Poised TSS	Skeletal Muscle Male	skeletal muscle
41	chr7:150019800-150020800	Active TSS	Primary T helper naive cells from peripheral blood	blood
42	chr7:150019800-150020800	Active TSS	Primary T killer memory cells from peripheral blood	blood
43	chr7:150019800-150020800	Active TSS	Brain Cingulate Gyrus	brain
44	chr7:150019800-150020800	Active TSS	Duodenum Mucosa	Duodenum
45	chr7:150019800-150021000	Active TSS	HUES64 Cell Line	embryonic stem cell
46	chr7:150019800-150021000	Active TSS	Breast Myoepithelial Primary Cells	Breast
47	chr7:150019800-150021000	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
48	chr7:150019800-150021000	Active TSS	Liver	Liver
49	chr7:150019800-150021000	Active TSS	Left Ventricle	heart
50	chr7:150019800-150021000	Active TSS	Dnd41	blood

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