Variant report

Variant	rs1916932
Chromosome Location	chr7:150021644-150021645
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:42)
CpG islands
(count:0)
Chromatin interactive
region (count:17)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:42 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	SMARCA4	chr7:150019611-150021724	K562	blood:	n/a	n/a
2	SREBP1	chr7:150019233-150021870	GM12878	blood:	n/a	n/a
3	SMC3	chr7:150020047-150021957	Hela-S3	cervix:	n/a	n/a
4	CHD2	chr7:150021584-150021729	Hela-S3	cervix:	n/a	n/a
5	NR2F2	chr7:150021549-150022158	K562	blood:	n/a	n/a
6	USF2	chr7:150021560-150021676	HepG2	liver:	n/a	n/a
7	TBP	chr7:150020056-150021925	Hela-S3	cervix:	n/a	n/a
8	GTF2F1	chr7:150021294-150021858	Hela-S3	cervix:	n/a	n/a
9	POLR2A	chr7:150018867-150022802	HepG2	liver:	n/a	n/a
10	UBTF	chr7:150019487-150021860	K562	blood:	n/a	n/a
11	HEY1	chr7:150021305-150021782	K562	blood:	n/a	n/a
12	JUND	chr7:150021258-150021654	K562	blood:	n/a	n/a
13	POLR2A	chr7:150021505-150022040	HepG2	liver:	n/a	n/a
14	ELF1	chr7:150021591-150022142	K562	blood:	n/a	n/a
15	POLR2A	chr7:150021110-150021961	Hela-S3	cervix:	n/a	n/a
16	NR2F2	chr7:150019069-150022252	K562	blood:	n/a	n/a
17	TBL1XR1	chr7:150021430-150021759	K562	blood:	n/a	n/a
18	TEAD4	chr7:150018830-150022115	K562	blood:	n/a	n/a
19	POLR2A	chr7:150021598-150022235	HepG2	liver:	n/a	n/a
20	POLR2A	chr7:150018976-150022034	Hela-S3	cervix:	n/a	n/a
21	MAX	chr7:150018987-150021981	K562	blood:	n/a	n/a
22	POLR2A	chr7:150021643-150021757	K562	blood:	n/a	n/a
23	POLR2A	chr7:150019144-150021977	Hela-S3	cervix:	n/a	n/a
24	POLR2A	chr7:150021596-150022004	HepG2	liver:	n/a	n/a
25	WRNIP1	chr7:150021521-150021898	GM12878	blood:	n/a	n/a
26	CTCF	chr7:150021500-150021650	GM12874	blood:	n/a	n/a
27	SPI1	chr7:150021510-150021816	GM12878	blood:	n/a	n/a
28	POLR2A	chr7:150019177-150021746	K562	blood:	n/a	n/a
29	HCFC1	chr7:150019674-150022174	Hela-S3	cervix:	n/a	n/a
30	TBP	chr7:150019356-150021766	K562	blood:	n/a	n/a
31	POLR2A	chr7:150021109-150022035	Hela-S3	cervix:	n/a	n/a
32	SMARCC2	chr7:150019950-150021665	Hela-S3	cervix:	n/a	n/a
33	STAT1	chr7:150018875-150022008	Hela-S3	cervix:	n/a	chr7:150021894-150021906 chr7:150019659-150019670
34	SPI1	chr7:150021528-150021750	K562	blood:	n/a	n/a
35	MAX	chr7:150021530-150021710	K562	blood:	n/a	n/a
36	SMARCC1	chr7:150019930-150022044	Hela-S3	cervix:	n/a	n/a
37	REST	chr7:150021641-150022011	K562	blood:	n/a	chr7:150021875-150021884
38	POLR2A	chr7:150021164-150021731	K562	blood:	n/a	n/a
39	POLR2A	chr7:150019128-150022034	K562	blood:	n/a	n/a
40	POLR2A	chr7:150019051-150022007	K562	blood:	n/a	n/a
41	MBD4	chr7:150021500-150021900	HepG2	liver:	n/a	n/a
42	POLR2A	chr7:150019000-150022112	Hela-S3	cervix:	n/a	n/a

No data

(count:17 , 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	chr7:150021516..150023885-chr7:150100772..150104958,4	K562	blood:
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	chr7:150018966..150021782-chr7:150094675..150098930,7	K562	blood:
10	chr7:150018539..150023441-chr7:150073756..150077036,7	MCF-7	breast:
11	chr7:150021038..150023907-chr7:150765022..150767583,2	MCF-7	breast:
12	chr7:150020472..150021986-chr7:150100705..150102934,2	MCF-7	breast:
13	chr7:150019910..150022890-chr7:150026315..150029098,3	MCF-7	breast:
14	chr7:150018458..150023402-chr7:150064103..150067772,7	MCF-7	breast:
15	chr7:150019591..150022356-chr7:150674947..150677441,2	K562	blood:
16	chr7:150017186..150022141-chr7:150063447..150068849,12	K562	blood:
17	chr7:150018966..150021939-chr7:150095611..150098750,5	K562	blood:

No data

Variant related genes	Relation type
ACTR3C	TF binding region
ENSG00000188707	Chromatin interaction
ENSG00000196456	Chromatin interaction
ENSG00000055118	Chromatin interaction
ENSG00000106538	Chromatin interaction
ENSG00000261305	Chromatin interaction
ENSG00000172493	Chromatin interaction
ENSG00000240449	Chromatin interaction
ENSG00000164889	Chromatin interaction
ENSG00000214022	Chromatin interaction

Extended variants
information (count: 80 )
Associated
traits (count: 19 )

rSNPs within LD-proxies of this variant (count:65)

rs_ID	r²[population]
rs10247016	0.80[ASN][1000 genomes]
rs1047207	0.84[EUR][1000 genomes]
rs1047575	0.81[EUR][1000 genomes]
rs1047586	0.80[EUR][1000 genomes]
rs10952249	0.88[EUR][1000 genomes]
rs10952250	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11764936	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11765644	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11765692	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11766288	0.82[EUR][1000 genomes]
rs11767726	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11769348	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11773351	0.90[EUR][1000 genomes]
rs11974980	0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11975886	0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11983355	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1464752	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1464753	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17173617	0.84[EUR][1000 genomes]
rs17837498	0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1962004	0.89[EUR][1000 genomes]
rs1983440	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2098053	0.82[EUR][1000 genomes]
rs2108851	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2108852	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2108853	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2108854	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2159234	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2159235	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2159236	0.80[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2373751	0.92[EUR][1000 genomes]
rs3088207	0.89[EUR][1000 genomes]
rs3735167	0.85[EUR][1000 genomes]
rs3735169	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs3735170	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs3735171	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs3735172	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3735173	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3735174	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3735175	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3800780	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs3800781	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4395803	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4554381	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs55715989	0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs55881542	0.91[EUR][1000 genomes]
rs55974958	0.84[EUR][1000 genomes]
rs56019796	0.86[AFR][1000 genomes];0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs56190213	0.91[EUR][1000 genomes]
rs56923535	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs56998970	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs57888387	0.85[EUR][1000 genomes]
rs59572505	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs60268791	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs60283368	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs60467296	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs61421252	0.84[EUR][1000 genomes]
rs6964110	0.82[EUR][1000 genomes]
rs73170169	0.85[EUR][1000 genomes]
rs73170174	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73170185	0.92[EUR][1000 genomes]
rs7781827	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7788316	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7806429	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs883138	0.80[EUR][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:19)

SNP	Gene	Cis/trans	Tissue	Source
rs1916932	LRRC61	cis	Adipose Subcutaneous	GTEx
rs1916932	ZBED6CL	cis	Esophagus Muscularis	GTEx
rs1916932	LRRC61	cis	Heart Left Ventricle	GTEx
rs1916932	LRRC61	cis	Artery Aorta	GTEx
rs1916932	LRRC61	cis	Stomach	GTEx
rs1916932	LRRC61	cis	lung	GTEx
rs1916932	LRRC61	cis	Whole Blood	GTEx
rs1916932	C7orf29	Cis_1M	lymphoblastoid	RTeQTL
rs1916932	LRRC61	cis	Skin Sun Exposed Lower leg	GTEx
rs1916932	LRRC61	Cis_1M	lymphoblastoid	RTeQTL
rs1916932	LRRC61	cis	Thyroid	GTEx
rs1916932	LRRC61	cis	Esophagus Mucosa	GTEx
rs1916932	ACTR3C	cis	Muscle Skeletal	GTEx
rs1916932	REPIN1	cis	Muscle Skeletal	GTEx
rs1916932	LRRC61	cis	Muscle Skeletal	GTEx
rs1916932	RARRES2	cis	multi-tissue	Pritchard
rs1916932	LRRC61	cis	Nerve Tibial	GTEx
rs1916932	LRRC61	cis	Artery Tibial	GTEx
rs1916932	ZBED6CL	cis	Esophagus Mucosa	GTEx

Chromatin state (count:112 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:150019000-150022000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr7:150019200-150022000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr7:150019200-150022000	Active TSS	Rectal Smooth Muscle	rectum
4	chr7:150019400-150021800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
5	chr7:150019400-150021800	Active TSS	Pancreatic Islets	Pancreatic Islet
6	chr7:150019600-150021800	Flanking Active TSS	Primary hematopoietic stem cells	blood
7	chr7:150019600-150022000	Flanking Active TSS	Adipose Nuclei	Adipose
8	chr7:150019600-150022000	Flanking Active TSS	Stomach Smooth Muscle	stomach
9	chr7:150019600-150022200	Flanking Active TSS	Primary B cells from cord blood	blood
10	chr7:150019800-150021800	Active TSS	ES-I3 Cell Line	embryonic stem cell
11	chr7:150019800-150021800	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr7:150020200-150021800	Active TSS	HUES48 Cell Line	embryonic stem cell
13	chr7:150020200-150021800	Bivalent/Poised TSS	HepG2	liver
14	chr7:150020400-150023000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr7:150020400-150030000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr7:150020600-150022200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr7:150020600-150023600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
18	chr7:150020800-150021800	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
19	chr7:150020800-150021800	Flanking Active TSS	Fetal Brain Male	brain
20	chr7:150020800-150021800	Flanking Active TSS	Fetal Lung	lung
21	chr7:150020800-150021800	Flanking Active TSS	Fetal Thymus	thymus
22	chr7:150020800-150021800	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
23	chr7:150020800-150022000	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
24	chr7:150020800-150022000	Flanking Active TSS	Colonic Mucosa	Colon
25	chr7:150020800-150022000	Flanking Active TSS	Duodenum Mucosa	Duodenum
26	chr7:150020800-150022200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
27	chr7:150020800-150022600	Enhancers	Spleen	Spleen
28	chr7:150020800-150022600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
29	chr7:150020800-150022800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr7:150020800-150023000	Enhancers	HSMM	muscle
31	chr7:150021000-150021800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr7:150021000-150021800	Enhancers	Placenta Amnion	Placenta Amnion
33	chr7:150021000-150022000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
34	chr7:150021000-150022000	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
35	chr7:150021000-150022000	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
36	chr7:150021000-150022000	Enhancers	HUVEC	blood vessel
37	chr7:150021000-150022200	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
38	chr7:150021000-150022400	Flanking Active TSS	Liver	Liver
39	chr7:150021000-150022400	Flanking Active TSS	Fetal Brain Female	brain
40	chr7:150021000-150022400	Enhancers	Skeletal Muscle Female	skeletal muscle
41	chr7:150021000-150022400	Transcr. at gene 5' and 3'	K562	blood
42	chr7:150021000-150022600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr7:150021200-150021800	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr7:150021200-150021800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
45	chr7:150021200-150021800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
46	chr7:150021200-150021800	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
47	chr7:150021200-150021800	Flanking Active TSS	Colon Smooth Muscle	Colon
48	chr7:150021200-150021800	Flanking Active TSS	Stomach Mucosa	stomach
49	chr7:150021200-150021800	Flanking Active TSS	Thymus	Thymus
50	chr7:150021200-150022000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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