Variant report

Variant	rs2285724
Chromosome Location	chr7:27227359-27227360
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:15)
CpG islands
(count:122)
Chromatin interactive
region (count:0)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:15 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr7:27210872-27233770	Hela-S3	cervix:	n/a	n/a
2	POLR2A	chr7:27226903-27229330	HUVEC	blood vessel:	n/a	n/a
3	CTCF	chr7:27227260-27227410	NB4	blood:	n/a	n/a
4	POLR2A	chr7:27227340-27229171	NB4	blood:	n/a	n/a
5	MAX	chr7:27227269-27227382	Hela-S3	cervix:	n/a	n/a
6	POLR2A	chr7:27227232-27230619	Hela-S3	cervix:	n/a	n/a
7	SMARCB1	chr7:27227109-27229609	Hela-S3	cervix:	n/a	n/a
8	SUZ12	chr7:27226938-27229675	H1-hESC	embryonic stem cell:	n/a	n/a
9	POLR2A	chr7:27227186-27229382	HUVEC	blood vessel:	n/a	n/a
10	BACH1	chr7:27227265-27227448	H1-hESC	embryonic stem cell:	n/a	n/a
11	SUZ12	chr7:27226717-27230090	NT2-D1	testis:	n/a	n/a
12	POLR2A	chr7:27227184-27229199	HUVEC	blood vessel:	n/a	n/a
13	CTBP2	chr7:27227146-27228914	H1-hESC	embryonic stem cell:	n/a	n/a
14	MAX	chr7:27227193-27228892	NB4	blood:	n/a	n/a
15	MYC	chr7:27227209-27228734	NB4	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:27227340-27227390	A549	lung:	n/a
2	chr7:27227358-27227408	ovcar-3	ovarian:	n/a
3	chr7:27227340-27227390	HRPEpiC	eye:	n/a
4	chr7:27227358-27227408	CMK	blood:	n/a
5	chr7:27227340-27227390	GM12878	blood:	n/a
6	chr7:27227358-27227408	BE2_C	brain:	n/a
7	chr7:27227340-27227390	T-47D	breast:	n/a
8	chr7:27227358-27227408	IMR90	lung:	fetal
9	chr7:27227358-27227408	MCF-7	breast:	n/a
10	chr7:27227340-27227390	BJ	skin:	n/a
11	chr7:27227340-27227390	SK-N-MC	brain:	n/a
12	chr7:27227358-27227408	GM12891	blood:	n/a
13	chr7:27227358-27227408	HMEC	breast:	n/a
14	chr7:27227358-27227408	HIPEpiC	eye:	n/a
15	chr7:27227358-27227408	HepG2	liver:	n/a
16	chr7:27227340-27227390	HRCEpiC	kidney:	n/a
17	chr7:27227340-27227390	HEK293	kidney:	embryo
18	chr7:27227340-27227390	SKMC	muscle:	n/a
19	chr7:27227340-27227390	HepG2	liver:	n/a
20	chr7:27227340-27227390	Hela-S3	cervix:	n/a
21	chr7:27227340-27227390	NHDF-neo	bronchial:	n/a
22	chr7:27227358-27227408	HEK293	kidney:	embryo
23	chr7:27227340-27227390	HCF	heart:	n/a
24	chr7:27227340-27227390	AoSMC	blood vessel:	n/a
25	chr7:27227358-27227408	PrEC	prostate:	n/a
26	chr7:27227358-27227408	K562	blood:	n/a
27	chr7:27227358-27227408	HAEpiC	amniotic membrane:	n/a
28	chr7:27227358-27227408	NHDF-neo	bronchial:	n/a
29	chr7:27227358-27227408	RPTEC	kidney:	n/a
30	chr7:27227358-27227408	GM12878	blood:	n/a
31	chr7:27227340-27227390	K562	blood:	n/a
32	chr7:27227358-27227408	AG09319	gingival:	n/a
33	chr7:27227358-27227408	T-47D	breast:	n/a
34	chr7:27227340-27227390	BE2_C	brain:	n/a
35	chr7:27227358-27227408	SK-N-MC	brain:	n/a
36	chr7:27227358-27227408	AG09309	skin:	n/a
37	chr7:27227340-27227390	AG09309	skin:	n/a
38	chr7:27227358-27227408	GM12892	blood:	n/a
39	chr7:27227358-27227408	AG10803	skin:	n/a
40	chr7:27227340-27227390	MCF-7	breast:	n/a
41	chr7:27227358-27227408	HCPEpiC	choroid plexus:	n/a
42	chr7:27227340-27227390	GM19239	blood:	n/a
43	chr7:27227358-27227408	MCF10A-Er-Src	breast:	n/a
44	chr7:27227358-27227408	H1-hESC	embryonic stem cell:	embryo
45	chr7:27227340-27227390	AG10803	skin:	n/a
46	chr7:27227340-27227390	HL-60	blood:	n/a
47	chr7:27227358-27227408	Caco-2	colon:	n/a
48	chr7:27227358-27227408	Jurkat	blood:	n/a
49	chr7:27227358-27227408	HCM	heart:	n/a
50	chr7:27227358-27227408	HEEpiC	esophagus:	n/a

No data

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HOXA13-1	chr7:27226866-27231685	XLOC_006390

No data

Variant related genes	Relation type
HOXA11	TF binding region
HOXA11-AS	TF binding region
HOXA11-AS	CpG island
HOXA11	CpG island

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs10233387	0.80[JPT][hapmap]
rs2023843	0.86[JPT][hapmap]
rs2023844	0.84[JPT][hapmap]
rs3735533	0.86[JPT][hapmap]
rs3807598	0.81[JPT][hapmap]
rs4722670	0.85[CHB][hapmap];0.86[JPT][hapmap];0.87[ASN][1000 genomes]
rs4722671	0.86[CHB][hapmap];0.84[ASN][1000 genomes]
rs4722672	0.82[ASN][1000 genomes]
rs4722675	0.81[JPT][hapmap]
rs6461995	0.86[CHB][hapmap];0.84[ASN][1000 genomes]
rs6968828	0.87[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.82[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs757181	0.86[JPT][hapmap];0.82[ASN][1000 genomes]
rs916880	0.85[CHB][hapmap];0.90[JPT][hapmap];0.87[ASN][1000 genomes]
rs929250	0.86[JPT][hapmap]
rs9770544	0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:41 , 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	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
4	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
5	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
6	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
7	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
8	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
9	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
10	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
11	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
12	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
13	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
14	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
15	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
16	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
17	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
18	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
19	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
20	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
21	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
22	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
23	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
24	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
25	nsv606468	chr7:27202289-27281304	Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Weak transcription Active TSS 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	135 gene(s)	inside rSNPs	diseases
26	nsv887880	chr7:27205282-27294701	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' Weak transcription Genic enhancers ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	132 gene(s)	inside rSNPs	diseases
27	nsv887881	chr7:27205282-27297791	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	132 gene(s)	inside rSNPs	diseases
28	nsv887882	chr7:27206688-27243962	Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Active TSS Transcr. at gene 5' and 3' Enhancers Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	128 gene(s)	inside rSNPs	diseases
29	nsv887883	chr7:27206688-27248373	Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Weak transcription Enhancers Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	128 gene(s)	inside rSNPs	diseases
30	nsv887884	chr7:27206688-27297791	Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	130 gene(s)	inside rSNPs	diseases
31	nsv1026327	chr7:27207777-27288521	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Enhancers Active TSS Weak 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	130 gene(s)	inside rSNPs	diseases
32	nsv538808	chr7:27207777-27288521	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	130 gene(s)	inside rSNPs	diseases
33	nsv887885	chr7:27208018-27274634	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Weak 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	128 gene(s)	inside rSNPs	diseases
34	nsv887886	chr7:27215041-27297791	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Enhancers Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	69 gene(s)	inside rSNPs	diseases
35	nsv887887	chr7:27217359-27252246	Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	65 gene(s)	inside rSNPs	diseases
36	nsv887888	chr7:27217746-27281157	Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Active TSS Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
37	nsv606469	chr7:27220831-27247279	Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
38	nsv887889	chr7:27220831-27297791	Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
39	nsv887890	chr7:27221137-27274634	Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
40	nsv887891	chr7:27223563-27264337	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	59 gene(s)	inside rSNPs	diseases
41	nsv887892	chr7:27223563-27297791	Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	61 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:60 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:27223400-27229200	Active TSS	Colon Smooth Muscle	Colon
2	chr7:27225000-27228200	Bivalent Enhancer	Primary T killer naive cells fromperipheralblood	blood
3	chr7:27225200-27228200	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
4	chr7:27225200-27229400	Flanking Active TSS	HUVEC	blood vessel
5	chr7:27225400-27227800	Weak transcription	Right Atrium	heart
6	chr7:27225400-27229000	Active TSS	HSMM	muscle
7	chr7:27225600-27228200	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr7:27225600-27228600	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr7:27225600-27229800	Flanking Active TSS	Muscle Satellite Cultured Cells	--
10	chr7:27225800-27227400	Bivalent Enhancer	Primary T cells from cord blood	blood
11	chr7:27225800-27227600	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr7:27225800-27227600	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
13	chr7:27225800-27229200	Active TSS	Rectal Smooth Muscle	rectum
14	chr7:27226000-27227400	Active TSS	Colonic Mucosa	Colon
15	chr7:27226000-27228000	Weak transcription	Pancreas	Pancrea
16	chr7:27226000-27229200	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
17	chr7:27226200-27227400	Active TSS	Rectal Mucosa Donor 29	rectum
18	chr7:27226400-27232400	Weak transcription	NHDF-Ad	bronchial
19	chr7:27226600-27227400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr7:27226800-27227400	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
21	chr7:27226800-27228000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
22	chr7:27226800-27228000	Bivalent/Poised TSS	Skeletal Muscle Male	skeletal muscle
23	chr7:27226800-27228200	Bivalent Enhancer	Primary T helper naive cells from peripheral blood	blood
24	chr7:27226800-27229400	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
25	chr7:27226800-27230000	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
26	chr7:27226800-27236000	Weak transcription	A549	lung
27	chr7:27227000-27227400	Bivalent Enhancer	Placenta	Placenta
28	chr7:27227000-27227600	Flanking Bivalent TSS/Enh	Hela-S3	cervix
29	chr7:27227000-27227800	Bivalent/Poised TSS	Skeletal Muscle Female	skeletal muscle
30	chr7:27227000-27228200	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
31	chr7:27227000-27228800	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr7:27227000-27228800	Bivalent/Poised TSS	Fetal Intestine Small	intestine
33	chr7:27227000-27229200	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
34	chr7:27227200-27227400	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells	blood
35	chr7:27227200-27227400	Flanking Bivalent TSS/Enh	Primary T helper naive cells fromperipheralblood	blood
36	chr7:27227200-27227400	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
37	chr7:27227200-27227400	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr7:27227200-27227400	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr7:27227200-27227400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr7:27227200-27227400	Enhancers	Gastric	stomach
41	chr7:27227200-27227400	Bivalent Enhancer	Dnd41	blood
42	chr7:27227200-27227400	Flanking Active TSS	HSMMtube	muscle
43	chr7:27227200-27227400	Flanking Active TSS	Osteobl	bone
44	chr7:27227200-27227600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr7:27227200-27227600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
46	chr7:27227200-27227600	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
47	chr7:27227200-27227800	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
48	chr7:27227200-27227800	Bivalent Enhancer	Primary T cells effector/memory enriched fromperipheralblood	blood
49	chr7:27227200-27228000	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
50	chr7:27227200-27228000	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 2	blood

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