Variant report

Variant	rs17437265
Chromosome Location	chr7:27163708-27163709
allele	G/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	CHD1	chr7:27152421-27165798	IMR90	lung:	n/a	n/a
2	MAX	chr7:27163459-27164406	HCT-116	colon:	n/a	chr7:27163770-27163779 chr7:27164323-27164332 chr7:27164323-27164332 chr7:27164323-27164332 chr7:27164321-27164334 chr7:27164318-27164327 chr7:27164321-27164334 chr7:27164321-27164334
3	RAD21	chr7:27163535-27164590	IMR90	lung:	n/a	chr7:27163543-27163555 chr7:27163545-27163555 chr7:27164415-27164428
4	SUZ12	chr7:27161567-27165692	H1-hESC	embryonic stem cell:	n/a	n/a
5	POLR2A	chr7:27163449-27164472	HUVEC	blood vessel:	n/a	n/a
6	POLR2A	chr7:27163633-27164223	U87	brain:	n/a	n/a
7	JUND	chr7:27163466-27164677	HCT-116	colon:	n/a	chr7:27163771-27163780 chr7:27163837-27163851 chr7:27163774-27163786 chr7:27164318-27164328 chr7:27164494-27164506
8	POLR2A	chr7:27160289-27163758	HepG2	liver:	n/a	n/a
9	TCF7L2	chr7:27163579-27164138	HCT-116	colon:	n/a	n/a
10	POLR2A	chr7:27163606-27164050	HUVEC	blood vessel:	n/a	n/a
11	JUND	chr7:27163445-27164351	HCT-116	colon:	n/a	chr7:27163771-27163780 chr7:27163837-27163851 chr7:27163774-27163786 chr7:27164318-27164328
12	CTCF	chr7:27163660-27164059	IMR90	lung:	n/a	n/a
13	FOSL1	chr7:27163516-27164681	HCT-116	colon:	n/a	chr7:27163771-27163780 chr7:27163837-27163851 chr7:27163774-27163786 chr7:27164318-27164328 chr7:27164494-27164506
14	POLR2A	chr7:27163352-27163708	HepG2	liver:	n/a	n/a
15	FOS	chr7:27163614-27164826	HUVEC	blood vessel:	n/a	chr7:27163771-27163780 chr7:27163837-27163851 chr7:27163774-27163786 chr7:27164318-27164328 chr7:27164494-27164506
16	POLR2A	chr7:27163637-27164080	HCT-116	colon:	n/a	n/a
17	YY1	chr7:27163685-27164010	HCT-116	colon:	n/a	chr7:27163814-27163828 chr7:27163820-27163829 chr7:27163815-27163829
18	POLR2A	chr7:27163426-27164681	HUVEC	blood vessel:	n/a	n/a
19	SUZ12	chr7:27161578-27165047	NT2-D1	testis:	n/a	n/a
20	GATA2	chr7:27163531-27164707	HUVEC	blood vessel:	n/a	chr7:27163714-27163724 chr7:27163715-27163724 chr7:27163715-27163722 chr7:27164379-27164396 chr7:27164453-27164461 chr7:27163712-27163722
21	POLR2A	chr7:27160061-27164901	IMR90	lung:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	7:27162022-27164727..7:27207968-27210222	H1-hESC	embryonic stem cell:	embryo
2	7:27162022-27164727..7:27181770-27195105	H1-hESC	embryonic stem cell:	embryo
3	7:27137201-27143270..7:27162022-27164727	H1-hESC	embryonic stem cell:	embryo
4	7:27162022-27164727..7:27176959-27181770	H1-hESC	embryonic stem cell:	embryo
5	7:27162022-27164727..7:27216170-27221403	H1-hESC	embryonic stem cell:	embryo
6	7:27162022-27164727..7:27238414-27242313	H1-hESC	embryonic stem cell:	embryo
7	7:27162022-27164727..7:27165488-27167947	H1-hESC	embryonic stem cell:	embryo
8	7:27162022-27164727..7:27203007-27207968	H1-hESC	embryonic stem cell:	embryo
9	chr7:27161653..27164579-chr7:27169154..27171048,2	MCF-7	breast:
10	7:27143270-27156413..7:27162022-27164727	H1-hESC	embryonic stem cell:	embryo
11	chr7:27163696..27168800-chr7:27169622..27172644,4	K562	blood:
12	7:27130634-27137201..7:27162022-27164727	H1-hESC	embryonic stem cell:	embryo

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EVX1-10	chr7:27163631-27163886	ENSG00000253552
2	lnc-EVX1-10	chr7:27163079-27164229	ENSG00000253552

Variant related genes	Relation type
HOXA3	TF binding region
ENSG00000273433	Chromatin interaction
ENSG00000253293	Chromatin interaction
ENSG00000105997	Chromatin interaction
ENSG00000253552	Chromatin interaction
ENSG00000254369	Chromatin interaction
ENSG00000253187	Chromatin interaction
ENSG00000272801	Chromatin interaction
ENSG00000078399	Chromatin interaction
ENSG00000106031	Chromatin interaction
ENSG00000243766	Chromatin interaction
ENSG00000207584	Chromatin interaction
ENSG00000257184	Chromatin interaction
ENSG00000106004	Chromatin interaction
ENSG00000105991	Chromatin interaction
ENSG00000105996	Chromatin interaction
ENSG00000197576	Chromatin interaction
ENSG00000106006	Chromatin interaction
ENSG00000233429	Chromatin interaction

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs17437251	1.00[CEU][hapmap];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs17437369	1.00[CEU][hapmap];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs17471860	1.00[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:37 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1025538	chr7:26482342-27376045	Enhancers Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	213 gene(s)	inside rSNPs	diseases
2	nsv538805	chr7:26482342-27376045	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Strong transcription Flanking Active TSS Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	213 gene(s)	inside rSNPs	diseases
3	nsv1018709	chr7:26990384-27216552	Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	140 gene(s)	inside rSNPs	diseases
4	nsv538806	chr7:26990384-27216552	Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Genic enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	140 gene(s)	inside rSNPs	diseases
5	nsv887856	chr7:27073731-27297791	Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	183 gene(s)	inside rSNPs	diseases
6	nsv824038	chr7:27119294-27284522	Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	183 gene(s)	inside rSNPs	diseases
7	nsv887857	chr7:27120689-27229549	Bivalent Enhancer Flanking Active TSS Active TSS Enhancers Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	176 gene(s)	inside rSNPs	diseases
8	nsv824039	chr7:27121825-27294951	Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	183 gene(s)	inside rSNPs	diseases
9	nsv824040	chr7:27121870-27295010	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	183 gene(s)	inside rSNPs	diseases
10	nsv887858	chr7:27127231-27188659	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
11	nsv887860	chr7:27127231-27196069	Weak transcription Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
12	nsv887859	chr7:27127231-27196113	Bivalent Enhancer Flanking Active TSS Weak transcription Bivalent/Poised TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
13	nsv887861	chr7:27127231-27206688	Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Active TSS Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	75 gene(s)	inside rSNPs	diseases
14	nsv887862	chr7:27127231-27217359	Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	141 gene(s)	inside rSNPs	diseases
15	nsv887863	chr7:27127231-27243106	Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	181 gene(s)	inside rSNPs	diseases
16	nsv887864	chr7:27127231-27243962	Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	181 gene(s)	inside rSNPs	diseases
17	nsv887865	chr7:27127231-27247279	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	181 gene(s)	inside rSNPs	diseases
18	nsv887866	chr7:27127231-27248373	Bivalent/Poised TSS Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	181 gene(s)	inside rSNPs	diseases
19	nsv887867	chr7:27127231-27252246	Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	181 gene(s)	inside rSNPs	diseases
20	nsv824041	chr7:27128039-27294951	Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	183 gene(s)	inside rSNPs	diseases
21	nsv606463	chr7:27135314-27182245	Active TSS Enhancers Genic enhancers Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
22	nsv887868	chr7:27135314-27202289	Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
23	nsv887869	chr7:27135314-27297791	Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	181 gene(s)	inside rSNPs	diseases
24	nsv887871	chr7:27136308-27179814	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
25	nsv887872	chr7:27136308-27181437	Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
26	nsv887873	chr7:27136308-27186495	Bivalent/Poised TSS Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
27	nsv887874	chr7:27136308-27196069	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
28	nsv606464	chr7:27138478-27168590	Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
29	nsv1020608	chr7:27139892-27324004	Bivalent Enhancer Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	182 gene(s)	inside rSNPs	diseases
30	nsv538807	chr7:27139892-27324004	Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	182 gene(s)	inside rSNPs	diseases
31	nsv1033316	chr7:27140645-27237951	Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	178 gene(s)	inside rSNPs	diseases
32	nsv606465	chr7:27143757-27229549	Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	174 gene(s)	inside rSNPs	diseases
33	nsv606466	chr7:27145024-27197319	Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
34	nsv606467	chr7:27145100-27196113	Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
35	nsv887875	chr7:27145100-27243962	Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	179 gene(s)	inside rSNPs	diseases
36	nsv532118	chr7:27146920-27354205	Flanking Active TSS Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	182 gene(s)	inside rSNPs	diseases
37	nsv5674	chr7:27152562-27197341	Bivalent Enhancer Weak transcription Active TSS Flanking Bivalent TSS/Enh Enhancers Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:65 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:27146400-27169600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr7:27152800-27169400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr7:27155600-27169400	Weak transcription	Hela-S3	cervix
4	chr7:27156200-27169200	Weak transcription	Osteobl	bone
5	chr7:27160200-27163800	Flanking Active TSS	HUVEC	blood vessel
6	chr7:27160400-27164400	Transcr. at gene 5' and 3'	Fetal Stomach	stomach
7	chr7:27161000-27164200	Flanking Active TSS	HMEC	breast
8	chr7:27161000-27165200	Weak transcription	Psoas Muscle	Psoas
9	chr7:27161200-27164000	Weak transcription	Skeletal Muscle Male	skeletal muscle
10	chr7:27161200-27165400	Weak transcription	Skeletal Muscle Female	skeletal muscle
11	chr7:27161200-27165600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr7:27161200-27166600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr7:27161400-27164000	Active TSS	Fetal Kidney	kidney
14	chr7:27161400-27164600	Active TSS	Duodenum Smooth Muscle	Duodenum
15	chr7:27161600-27164000	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
16	chr7:27161600-27164200	Active TSS	Esophagus	oesophagus
17	chr7:27161600-27164400	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr7:27161600-27164600	Transcr. at gene 5' and 3'	Fetal Intestine Small	intestine
19	chr7:27161600-27166200	Genic enhancers	Fetal Muscle Leg	muscle
20	chr7:27161800-27164000	Weak transcription	Small Intestine	intestine
21	chr7:27161800-27164400	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
22	chr7:27161800-27164600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr7:27161800-27164800	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
24	chr7:27162000-27163800	Flanking Active TSS	NHLF	lung
25	chr7:27162000-27164200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr7:27162200-27164200	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr7:27162200-27164200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr7:27162200-27169000	Weak transcription	NHEK	skin
29	chr7:27162400-27163800	Weak transcription	Pancreas	Pancrea
30	chr7:27162400-27164200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr7:27162400-27165200	Weak transcription	Right Atrium	heart
32	chr7:27162400-27165800	Weak transcription	Primary hematopoietic stem cells	blood
33	chr7:27162600-27169000	Weak transcription	Muscle Satellite Cultured Cells	--
34	chr7:27162600-27169000	Weak transcription	Aorta	Aorta
35	chr7:27162800-27163800	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
36	chr7:27162800-27164400	Enhancers	Sigmoid Colon	Sigmoid Colon
37	chr7:27162800-27169600	Flanking Active TSS	Stomach Smooth Muscle	stomach
38	chr7:27163000-27164600	Flanking Active TSS	Fetal Intestine Large	intestine
39	chr7:27163000-27164600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
40	chr7:27163000-27165000	Enhancers	Stomach Mucosa	stomach
41	chr7:27163200-27163800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr7:27163200-27163800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr7:27163200-27163800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
44	chr7:27163200-27163800	Flanking Active TSS	Rectal Smooth Muscle	rectum
45	chr7:27163200-27164000	Bivalent Enhancer	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr7:27163200-27164400	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
47	chr7:27163200-27165000	Weak transcription	Fetal Thymus	thymus
48	chr7:27163200-27170600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
49	chr7:27163400-27163800	Weak transcription	Adipose Nuclei	Adipose
50	chr7:27163400-27163800	Flanking Active TSS	Colon Smooth Muscle	Colon

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