Variant report

Variant	rs10238095
Chromosome Location	chr7:27196643-27196644
allele	A/G
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	POLR2A	chr7:27195561-27196842	HEK293	kidney:	n/a	n/a
2	POLR2A	chr7:27194513-27197277	HUVEC	blood vessel:	n/a	n/a
3	POLR2A	chr7:27196640-27196651	MCF-7	breast:	n/a	n/a
4	SUZ12	chr7:27192795-27199379	H1-hESC	embryonic stem cell:	n/a	n/a
5	POLR2A	chr7:27195502-27196830	HCT-116	colon:	n/a	n/a
6	TCF12	chr7:27195438-27196667	ECC-1	luminal epithelium:	n/a	chr7:27196482-27196489
7	USF1	chr7:27195393-27196736	HCT-116	colon:	n/a	chr7:27196303-27196314 chr7:27196290-27196303 chr7:27196292-27196301 chr7:27196293-27196302 chr7:27196292-27196301 chr7:27196356-27196372 chr7:27196291-27196302
8	POLR2A	chr7:27195051-27196830	Hela-S3	cervix:	n/a	n/a
9	TAF1	chr7:27195396-27196718	ECC-1	luminal epithelium:	n/a	n/a
10	USF1	chr7:27195394-27196651	ECC-1	luminal epithelium:	n/a	chr7:27196303-27196314 chr7:27196290-27196303 chr7:27196292-27196301 chr7:27196293-27196302 chr7:27196292-27196301 chr7:27196356-27196372 chr7:27196291-27196302
11	MAX	chr7:27195362-27196963	HCT-116	colon:	n/a	chr7:27196292-27196301 chr7:27196291-27196302 chr7:27195650-27195659
12	ZBTB7A	chr7:27196108-27196768	ECC-1	luminal epithelium:	n/a	n/a
13	FOXP2	chr7:27196631-27197141	SK-N-MC	brain:	n/a	n/a
14	USF1	chr7:27195525-27196694	HCT-116	colon:	n/a	chr7:27196303-27196314 chr7:27196290-27196303 chr7:27196292-27196301 chr7:27196293-27196302 chr7:27196292-27196301 chr7:27196356-27196372 chr7:27196291-27196302
15	ZNF263	chr7:27196624-27196952	HEK293-T-REx	kidney:	n/a	n/a
16	MAX	chr7:27195683-27196983	HUVEC	blood vessel:	n/a	chr7:27196292-27196301 chr7:27196291-27196302
17	POLR2A	chr7:27194531-27197239	HUVEC	blood vessel:	n/a	n/a
18	POLR2A	chr7:27196565-27196880	ECC-1	luminal epithelium:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:27194885..27197425-chr7:27205763..27208498,2	K562	blood:

Variant related genes	Relation type
ENSG00000272801	TF binding region
HOXA7	TF binding region
HOXA3	TF binding region
ENSG00000273433	TF binding region
ENSG00000270182	TF binding region
ENSG00000253187	Chromatin interaction

Extended variants
information (count: 86 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs10085570	0.93[ASN][1000 genomes]
rs10225507	0.81[ASN][1000 genomes]
rs10246712	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11564055	0.89[ASN][1000 genomes]
rs11762730	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11983200	0.88[ASN][1000 genomes]
rs12530948	1.00[ASN][1000 genomes]
rs12533947	0.91[ASN][1000 genomes]
rs12666919	1.00[ASN][1000 genomes]
rs12666926	1.00[ASN][1000 genomes]
rs1548497	0.93[ASN][1000 genomes]
rs1725074	0.87[ASN][1000 genomes]
rs17449108	0.91[ASN][1000 genomes]
rs17471485	0.91[ASN][1000 genomes]
rs17471520	0.94[ASN][1000 genomes]
rs1801085	0.93[ASN][1000 genomes]
rs1859166	0.93[ASN][1000 genomes]
rs2107063	0.93[ASN][1000 genomes]
rs2285722	0.90[ASN][1000 genomes]
rs2301720	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2301721	0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2428432	0.89[ASN][1000 genomes]
rs2428433	0.89[ASN][1000 genomes]
rs2428434	0.90[ASN][1000 genomes]
rs2465275	0.89[ASN][1000 genomes]
rs2465276	0.90[ASN][1000 genomes]
rs3735530	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3801320	0.93[ASN][1000 genomes]
rs3823764	0.93[ASN][1000 genomes]
rs4722657	0.93[ASN][1000 genomes]
rs4722659	0.93[ASN][1000 genomes]
rs4722666	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs61384251	0.90[ASN][1000 genomes]
rs6461985	0.93[ASN][1000 genomes]
rs6461987	0.94[ASN][1000 genomes]
rs68021164	0.97[ASN][1000 genomes]
rs6948297	0.93[ASN][1000 genomes]
rs6957209	0.93[ASN][1000 genomes]
rs6962314	0.94[ASN][1000 genomes]
rs6969780	0.93[ASN][1000 genomes]
rs6973182	0.94[ASN][1000 genomes]
rs6976129	0.94[ASN][1000 genomes]
rs73071548	0.93[ASN][1000 genomes]
rs73071550	0.93[ASN][1000 genomes]
rs7341470	0.97[ASN][1000 genomes]
rs739734	0.94[ASN][1000 genomes]
rs7798733	0.93[ASN][1000 genomes]
rs875898	0.95[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs886339	1.00[ASN][1000 genomes]
rs929249	0.94[ASN][1000 genomes]
rs983184	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs983185	0.96[AFR][1000 genomes];0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs985652	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:33 , 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	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
11	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
12	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
13	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
14	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
15	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
16	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
17	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
18	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
19	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
20	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
21	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
22	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
23	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
24	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
25	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
26	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
27	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
28	nsv824042	chr7:27169231-27247232	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS Genic enhancers 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	157 gene(s)	inside rSNPs	diseases
29	nsv887877	chr7:27169388-27217359	Bivalent Enhancer Bivalent/Poised TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription 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	115 gene(s)	inside rSNPs	diseases
30	nsv887878	chr7:27175295-27214557	Flanking Bivalent TSS/Enh Active TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	105 gene(s)	inside rSNPs	diseases
31	nsv887879	chr7:27175295-27297791	Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	151 gene(s)	inside rSNPs	diseases
32	esv1798853	chr7:27181568-27309266	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	150 gene(s)	inside rSNPs	diseases
33	nsv531024	chr7:27194426-27461954	Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active 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	148 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs10238095	HOXA2	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:70 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:27186800-27202600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr7:27193200-27197800	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
3	chr7:27193400-27200400	Flanking Active TSS	Primary hematopoietic stem cells	blood
4	chr7:27193600-27198600	Active TSS	Fetal Kidney	kidney
5	chr7:27194200-27197400	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr7:27194400-27196800	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
7	chr7:27194600-27196800	Bivalent Enhancer	Spleen	Spleen
8	chr7:27194800-27196800	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr7:27195000-27196800	Bivalent/Poised TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr7:27195200-27196800	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
11	chr7:27195200-27196800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr7:27195200-27196800	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr7:27195200-27197000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr7:27195200-27198400	Bivalent/Poised TSS	Small Intestine	intestine
15	chr7:27195400-27196800	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
16	chr7:27195400-27196800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr7:27195400-27196800	Active TSS	Psoas Muscle	Psoas
18	chr7:27195400-27196800	Active TSS	HSMMtube	muscle
19	chr7:27195400-27197000	Active TSS	Hela-S3	cervix
20	chr7:27195400-27198400	Active TSS	Rectal Mucosa Donor 31	rectum
21	chr7:27195400-27198600	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr7:27195400-27199600	Active TSS	Colonic Mucosa	Colon
23	chr7:27195400-27203200	Active TSS	Rectal Smooth Muscle	rectum
24	chr7:27195600-27196800	Bivalent Enhancer	Primary T helper naive cells from peripheral blood	blood
25	chr7:27195600-27196800	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr7:27195600-27196800	Bivalent/Poised TSS	Fetal Lung	lung
27	chr7:27195600-27196800	Active TSS	Rectal Mucosa Donor 29	rectum
28	chr7:27195600-27196800	Active TSS	Osteobl	bone
29	chr7:27195600-27200600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
30	chr7:27195800-27197200	Active TSS	Sigmoid Colon	Sigmoid Colon
31	chr7:27196000-27196800	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
32	chr7:27196000-27196800	Bivalent Enhancer	Right Ventricle	heart
33	chr7:27196200-27197000	Active TSS	Skeletal Muscle Female	skeletal muscle
34	chr7:27196200-27197200	Bivalent/Poised TSS	Primary T cells from cord blood	blood
35	chr7:27196200-27197600	Bivalent/Poised TSS	Fetal Intestine Large	intestine
36	chr7:27196200-27198400	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
37	chr7:27196200-27198600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
38	chr7:27196400-27196800	Bivalent Enhancer	Duodenum Smooth Muscle	Duodenum
39	chr7:27196400-27196800	Enhancers	Lung	lung
40	chr7:27196400-27197000	Bivalent Enhancer	Placenta	Placenta
41	chr7:27196400-27197800	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
42	chr7:27196400-27198400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr7:27196400-27198600	Bivalent Enhancer	Fetal Thymus	thymus
44	chr7:27196400-27199800	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
45	chr7:27196400-27199800	Weak transcription	Pancreas	Pancrea
46	chr7:27196600-27196800	Flanking Bivalent TSS/Enh	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr7:27196600-27196800	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr7:27196600-27196800	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
49	chr7:27196600-27196800	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
50	chr7:27196600-27196800	Flanking Active TSS	Muscle Satellite Cultured Cells	--

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