Variant report

Variant	rs55759700
Chromosome Location	chr7:27241295-27241296
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:8)
CpG islands
(count:61)
Chromatin interactive
region (count:3)
LncRNA
region (count:16)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:8 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	SPI1	chr7:27240532-27241404	HL-60	blood:	n/a	n/a
2	SUZ12	chr7:27237150-27242322	NT2-D1	testis:	n/a	n/a
3	SPI1	chr7:27240903-27241313	GM12891	blood:	n/a	n/a
4	POLR2A	chr7:27238513-27241847	NB4	blood:	n/a	n/a
5	MAX	chr7:27239576-27242108	NB4	blood:	n/a	chr7:27239844-27239854
6	SUZ12	chr7:27237874-27242333	H1-hESC	embryonic stem cell:	n/a	n/a
7	SPI1	chr7:27240622-27241362	GM12878	blood:	n/a	n/a
8	MYC	chr7:27239543-27241860	NB4	blood:	n/a	chr7:27239844-27239854

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:27241279-27241329	HEEpiC	esophagus:	n/a
2	chr7:27241279-27241329	HepG2	liver:	n/a
3	chr7:27241279-27241329	H1-hESC	embryonic stem cell:	embryo
4	chr7:27241279-27241329	MCF10A-Er-Src	breast:	n/a
5	chr7:27241279-27241329	GM12892	blood:	n/a
6	chr7:27241279-27241329	SK-N-SH	brain:	n/a
7	chr7:27241279-27241329	AG04450	lung:	fetal
8	chr7:27241279-27241329	Caco-2	colon:	n/a
9	chr7:27241279-27241329	U87	brain:	n/a
10	chr7:27241279-27241329	HNPCEpiC	eye:	n/a
11	chr7:27241279-27241329	ECC-1	luminal epithelium:	n/a
12	chr7:27241279-27241329	HRPEpiC	eye:	n/a
13	chr7:27241279-27241329	ProgFib	skin:	n/a
14	chr7:27241279-27241329	Hela-S3	cervix:	n/a
15	chr7:27241279-27241329	AG10803	skin:	n/a
16	chr7:27241279-27241329	LNCaP	prostate:	n/a
17	chr7:27241279-27241329	ovcar-3	ovarian:	n/a
18	chr7:27241279-27241329	HUVEC	blood vessel:	n/a
19	chr7:27241279-27241329	HRE	kidney:	n/a
20	chr7:27241279-27241329	SK-N-SH_RA	brain:	n/a
21	chr7:27241279-27241329	SK-N-MC	brain:	n/a
22	chr7:27241279-27241329	GM19239	blood:	n/a
23	chr7:27241279-27241329	IMR90	lung:	fetal
24	chr7:27241279-27241329	T-47D	breast:	n/a
25	chr7:27241279-27241329	HL-60	blood:	n/a
26	chr7:27241279-27241329	AG09309	skin:	n/a
27	chr7:27241279-27241329	HCT-116	colon:	n/a
28	chr7:27241279-27241329	GM06990	blood:	n/a
29	chr7:27241279-27241329	PANC-1	pancreas:	n/a
30	chr7:27241279-27241329	SAEC	small airway:	n/a
31	chr7:27241279-27241329	BE2_C	brain:	n/a
32	chr7:27241279-27241329	AG04449	skin:	fetal
33	chr7:27241279-27241329	AoSMC	blood vessel:	n/a
34	chr7:27241279-27241329	NHBE	bronchial:	n/a
35	chr7:27241279-27241329	RPTEC	kidney:	n/a
36	chr7:27241279-27241329	HIPEpiC	eye:	n/a
37	chr7:27241279-27241329	NH-A	brain:	n/a
38	chr7:27241279-27241329	NB4	blood:	n/a
39	chr7:27241279-27241329	MCF-7	breast:	n/a
40	chr7:27241279-27241329	HRCEpiC	kidney:	n/a
41	chr7:27241279-27241329	HCM	heart:	n/a
42	chr7:27241279-27241329	HPAEpiC	pulmonary alveolar:	n/a
43	chr7:27241279-27241329	HCF	heart:	n/a
44	chr7:27241279-27241329	Jurkat	blood:	n/a
45	chr7:27241279-27241329	GM12878	blood:	n/a
46	chr7:27241279-27241329	PrEC	prostate:	n/a
47	chr7:27241279-27241329	HEK293	kidney:	embryo
48	chr7:27241279-27241329	NT2-D1	testis:	n/a
49	chr7:27241279-27241329	K562	blood:	n/a
50	chr7:27241279-27241329	HAEpiC	amniotic membrane:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	7:27162022-27164727..7:27238414-27242313	H1-hESC	embryonic stem cell:	embryo
2	7:27061277-27071265..7:27238414-27242313	Hela-S3	cervix:
3	chr7:27232082..27233586-chr7:27238989..27241639,2	MCF-7	breast:

(count:16 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EVX1-3	chr7:27240242-27241306	ENSG00000243766
2	lnc-EVX1-3	chr7:27240242-27241306	ENSG00000243766
3	lnc-EVX1-3	chr7:27240242-27241306	ENSG00000243766
4	lnc-EVX1-3	chr7:27240242-27241306	ENSG00000243766
5	lnc-EVX1-3	chr7:27240242-27241306	ENSG00000243766
6	lnc-EVX1-3	chr7:27240242-27242441	ENSG00000243766
7	lnc-EVX1-3	chr7:27240242-27242441	ENSG00000243766
8	lnc-EVX1-3	chr7:27240242-27242441	ENSG00000243766
9	lnc-EVX1-3	chr7:27240242-27242441	ENSG00000243766
10	lnc-EVX1-3	chr7:27240242-27242441	ENSG00000243766
11	lnc-EVX1-3	chr7:27240242-27242257	NR_037843
12	lnc-EVX1-3	chr7:27240242-27241442	ENSG00000243766.3
13	lnc-EVX1-3	chr7:27240242-27241442	ENSG00000243766.3
14	lnc-EVX1-3	chr7:27240242-27241442	ENSG00000243766.3
15	lnc-EVX1-3	chr7:27240242-27241442	ENSG00000243766.3
16	lnc-EVX1-3	chr7:27240242-27241442	ENSG00000243766.3

No data

Variant related genes	Relation type
HOXA13	TF binding region
HOXA13	CpG island
ENSG00000214869	Chromatin interaction
ENSG00000266055	Chromatin interaction
ENSG00000253552	Chromatin interaction
ENSG00000253508	Chromatin interaction
HOXA9	LncRNA region
HOXA10	LncRNA region
HOXA13	LncRNA region
HOXA7	LncRNA region
HOXA11	LncRNA region

Extended variants
information (count: 64 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs17472315	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17472322	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17472378	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17472399	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17472420	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17472455	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17472532	1.00[AMR][1000 genomes]
rs17501174	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17501188	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17501195	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17501229	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17501236	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17501243	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17501271	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56184225	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60088802	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73683712	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73683713	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73683714	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73683715	1.00[AMR][1000 genomes]
rs73683716	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73683717	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73683718	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73683719	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73683720	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:39 , 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	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
6	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
7	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
8	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
9	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
10	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
11	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
12	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
13	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
14	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
15	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
16	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
17	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
18	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
19	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
20	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
21	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
22	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
23	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
24	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
25	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
26	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
27	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
28	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
29	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
30	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
31	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
32	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
33	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
34	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
35	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
36	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
37	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
38	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
39	esv3359129	chr7:27238452-27241300	Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:75 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:27238600-27242200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
2	chr7:27239600-27242000	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
3	chr7:27239800-27241400	Bivalent Enhancer	Fetal Stomach	stomach
4	chr7:27239800-27241400	Enhancers	Lung	lung
5	chr7:27239800-27241400	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
6	chr7:27239800-27242400	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
7	chr7:27240000-27241400	Bivalent Enhancer	Primary T killer memory cells from peripheral blood	blood
8	chr7:27240000-27241400	Flanking Bivalent TSS/Enh	Adipose Nuclei	Adipose
9	chr7:27240000-27241400	Flanking Bivalent TSS/Enh	Duodenum Mucosa	Duodenum
10	chr7:27240000-27241400	Flanking Bivalent TSS/Enh	HepG2	liver
11	chr7:27240200-27241400	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr7:27240200-27241400	Bivalent Enhancer	Primary T cells effector/memory enriched fromperipheralblood	blood
13	chr7:27240200-27241400	Flanking Bivalent TSS/Enh	Colon Smooth Muscle	Colon
14	chr7:27240200-27242000	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr7:27240200-27242200	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr7:27240200-27242200	Bivalent Enhancer	Primary T killer naive cells fromperipheralblood	blood
17	chr7:27240200-27242200	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
18	chr7:27240200-27242200	Enhancers	Pancreas	Pancrea
19	chr7:27240200-27242400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
20	chr7:27240200-27242400	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
21	chr7:27240400-27241400	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
22	chr7:27240400-27241400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr7:27240400-27241400	Enhancers	Spleen	Spleen
24	chr7:27240400-27241600	Bivalent Enhancer	Primary T helper naive cells fromperipheralblood	blood
25	chr7:27240400-27241600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr7:27240400-27241800	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
27	chr7:27240400-27241800	Enhancers	Ovary	ovary
28	chr7:27240400-27242000	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
29	chr7:27240400-27242000	Bivalent Enhancer	Brain Cingulate Gyrus	brain
30	chr7:27240400-27242200	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
31	chr7:27240400-27242200	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
32	chr7:27240400-27242200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
33	chr7:27240400-27242200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
34	chr7:27240400-27242200	Bivalent Enhancer	Fetal Muscle Leg	muscle
35	chr7:27240400-27242400	Bivalent Enhancer	Brain Dorsolateral Prefrontal Cortex	brain
36	chr7:27240600-27241400	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells short term culture	blood
37	chr7:27240600-27241400	Bivalent Enhancer	Primary T helper naive cells from peripheral blood	blood
38	chr7:27240600-27241400	Bivalent/Poised TSS	HMEC	breast
39	chr7:27240600-27241600	Flanking Bivalent TSS/Enh	Primary neutrophils fromperipheralblood	blood
40	chr7:27240600-27241600	Bivalent Enhancer	Duodenum Smooth Muscle	Duodenum
41	chr7:27240600-27241600	Bivalent Enhancer	HUVEC	blood vessel
42	chr7:27240600-27241800	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
43	chr7:27240600-27242200	Bivalent/Poised TSS	Fetal Intestine Small	intestine
44	chr7:27240600-27246200	Bivalent/Poised TSS	Rectal Smooth Muscle	rectum
45	chr7:27240800-27241400	Flanking Bivalent TSS/Enh	Primary monocytes fromperipheralblood	blood
46	chr7:27240800-27241400	Flanking Bivalent TSS/Enh	Primary B cells from cord blood	blood
47	chr7:27240800-27241400	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr7:27240800-27241400	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr7:27240800-27241400	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr7:27240800-27241400	Enhancers	A549	lung

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