Variant report

Variant	rs2075702
Chromosome Location	chr6:31937511-31937512
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:65)
CpG islands
(count:122)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	EP300	chr6:31937368-31937791	K562	blood:	n/a	chr6:31937561-31937570
2	MAX	chr6:31937406-31937769	K562	blood:	n/a	chr6:31937561-31937570
3	USF2	chr6:31937104-31938303	Hela-S3	cervix:	n/a	n/a
4	POLR2A	chr6:31937359-31938841	GM12878	blood:	n/a	n/a
5	BACH1	chr6:31937476-31937756	K562	blood:	n/a	n/a
6	POLR2A	chr6:31937284-31941234	K562	blood:	n/a	n/a
7	NR2F2	chr6:31937374-31937927	K562	blood:	n/a	n/a
8	POLR2A	chr6:31937428-31937890	K562	blood:	n/a	n/a
9	RAD21	chr6:31937491-31937655	IMR90	lung:	n/a	n/a
10	MAX	chr6:31937304-31937916	K562	blood:	n/a	chr6:31937561-31937570
11	POLR2A	chr6:31937431-31941001	GM12892	blood:	n/a	n/a
12	POLR2A	chr6:31937473-31940648	PANC-1	pancreas:	n/a	n/a
13	POLR2A	chr6:31937360-31941122	HepG2	liver:	n/a	n/a
14	POLR2A	chr6:31935907-31941545	HepG2	liver:	n/a	n/a
15	POLR2A	chr6:31936260-31941395	K562	blood:	n/a	n/a
16	POLR2A	chr6:31937353-31941181	K562	blood:	n/a	n/a
17	MAZ	chr6:31937466-31937862	K562	blood:	n/a	chr6:31937561-31937570
18	POLR2A	chr6:31935432-31941169	K562	blood:	n/a	n/a
19	TEAD4	chr6:31937298-31937926	K562	blood:	n/a	n/a
20	POLR2A	chr6:31937171-31940595	HepG2	liver:	n/a	n/a
21	POLR2A	chr6:31936378-31937526	GM12878	blood:	n/a	n/a
22	IRF1	chr6:31937449-31937742	K562	blood:	n/a	n/a
23	BHLHE40	chr6:31937444-31937713	K562	blood:	n/a	n/a
24	REST	chr6:31937379-31937824	K562	blood:	n/a	n/a
25	POLR2A	chr6:31937309-31938657	K562	blood:	n/a	n/a
26	TAL1	chr6:31937422-31937800	K562	blood:	n/a	n/a
27	POLR2A	chr6:31936682-31940672	PFSK-1	brain:	n/a	n/a
28	POLR2A	chr6:31936493-31941269	GM12892	blood:	n/a	n/a
29	POLR2A	chr6:31937408-31940545	PANC-1	pancreas:	n/a	n/a
30	NR2F2	chr6:31937432-31937868	K562	blood:	n/a	n/a
31	MAFK	chr6:31937319-31937847	K562	blood:	n/a	chr6:31937561-31937571
32	TBL1XR1	chr6:31937453-31937644	K562	blood:	n/a	n/a
33	POLR2A	chr6:31936820-31941128	GM12891	blood:	n/a	n/a
34	MAX	chr6:31937402-31937880	K562	blood:	n/a	chr6:31937561-31937570
35	JUN	chr6:31937392-31937868	K562	blood:	n/a	chr6:31937561-31937569 chr6:31937561-31937569 chr6:31937559-31937571 chr6:31937561-31937568 chr6:31937560-31937570
36	ARID3A	chr6:31937414-31937793	K562	blood:	n/a	n/a
37	POLR2A	chr6:31937483-31941074	HepG2	liver:	n/a	n/a
38	MYC	chr6:31937450-31937703	K562	blood:	n/a	chr6:31937561-31937570
39	MAFF	chr6:31937385-31937828	K562	blood:	n/a	n/a
40	JUN	chr6:31936988-31938663	K562	blood:	n/a	chr6:31937561-31937569 chr6:31937561-31937569 chr6:31937559-31937571 chr6:31937561-31937568 chr6:31937560-31937570
41	TAF1	chr6:31937431-31937871	K562	blood:	n/a	n/a
42	POLR2A	chr6:31934246-31941332	GM12878	blood:	n/a	n/a
43	CBX3	chr6:31937323-31938185	K562	blood:	n/a	n/a
44	POLR2A	chr6:31937489-31940892	H1-hESC	embryonic stem cell:	n/a	n/a
45	POLR2A	chr6:31937449-31937551	MCF-7	breast:	n/a	n/a
46	POLR2A	chr6:31937180-31941267	GM12892	blood:	n/a	n/a
47	RCOR1	chr6:31937495-31937825	K562	blood:	n/a	n/a
48	RCOR1	chr6:31937353-31937876	K562	blood:	n/a	n/a
49	ZNF263	chr6:31937474-31939008	HEK293-T-REx	kidney:	n/a	n/a
50	JUN	chr6:31937440-31937837	K562	blood:	n/a	chr6:31937561-31937569 chr6:31937561-31937569 chr6:31937559-31937571 chr6:31937561-31937568 chr6:31937560-31937570

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:31937470-31937520	SK-N-SH	brain:	n/a
2	chr6:31937462-31937512	PrEC	prostate:	n/a
3	chr6:31937470-31937520	GM12878	blood:	n/a
4	chr6:31937470-31937520	AG04450	lung:	fetal
5	chr6:31937470-31937520	NB4	blood:	n/a
6	chr6:31937462-31937512	SAEC	small airway:	n/a
7	chr6:31937470-31937520	NHBE	bronchial:	n/a
8	chr6:31937462-31937512	HCF	heart:	n/a
9	chr6:31937470-31937520	AG04449	skin:	fetal
10	chr6:31937462-31937512	GM06990	blood:	n/a
11	chr6:31937462-31937512	CMK	blood:	n/a
12	chr6:31937470-31937520	SK-N-SH_RA	brain:	n/a
13	chr6:31937462-31937512	H1-hESC	embryonic stem cell:	embryo
14	chr6:31937470-31937520	ProgFib	skin:	n/a
15	chr6:31937470-31937520	AG09319	gingival:	n/a
16	chr6:31937462-31937512	HL-60	blood:	n/a
17	chr6:31937462-31937512	U87	brain:	n/a
18	chr6:31937462-31937512	HMEC	breast:	n/a
19	chr6:31937462-31937512	HIPEpiC	eye:	n/a
20	chr6:31937470-31937520	BJ	skin:	n/a
21	chr6:31937470-31937520	SAEC	small airway:	n/a
22	chr6:31937462-31937512	SKMC	muscle:	n/a
23	chr6:31937470-31937520	HRCEpiC	kidney:	n/a
24	chr6:31937470-31937520	HCPEpiC	choroid plexus:	n/a
25	chr6:31937462-31937512	HRCEpiC	kidney:	n/a
26	chr6:31937470-31937520	LNCaP	prostate:	n/a
27	chr6:31937462-31937512	GM12891	blood:	n/a
28	chr6:31937470-31937520	AG10803	skin:	n/a
29	chr6:31937462-31937512	HCT-116	colon:	n/a
30	chr6:31937470-31937520	PFSK-1	brain:	n/a
31	chr6:31937462-31937512	ECC-1	luminal epithelium:	n/a
32	chr6:31937470-31937520	GM12892	blood:	n/a
33	chr6:31937462-31937512	ProgFib	skin:	n/a
34	chr6:31937470-31937520	HEK293	kidney:	embryo
35	chr6:31937462-31937512	ovcar-3	ovarian:	n/a
36	chr6:31937462-31937512	HAEpiC	amniotic membrane:	n/a
37	chr6:31937462-31937512	HPAEpiC	pulmonary alveolar:	n/a
38	chr6:31937470-31937520	NH-A	brain:	n/a
39	chr6:31937462-31937512	AoSMC	blood vessel:	n/a
40	chr6:31937470-31937520	HNPCEpiC	eye:	n/a
41	chr6:31937462-31937512	NHBE	bronchial:	n/a
42	chr6:31937470-31937520	GM12891	blood:	n/a
43	chr6:31937462-31937512	Hela-S3	cervix:	n/a
44	chr6:31937462-31937512	AG04450	lung:	fetal
45	chr6:31937470-31937520	ECC-1	luminal epithelium:	n/a
46	chr6:31937462-31937512	HepG2	liver:	n/a
47	chr6:31937462-31937512	A549	lung:	n/a
48	chr6:31937462-31937512	HNPCEpiC	eye:	n/a
49	chr6:31937470-31937520	HAEpiC	amniotic membrane:	n/a
50	chr6:31937462-31937512	MCF-7	breast:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:56708053..56710341-chr6:31937045..31938607,2	MCF-7	breast:
2	chr6:31864068..31872693-chr6:31934470..31941847,12	MCF-7	breast:
3	chr6:31802718..31804825-chr6:31935287..31937664,2	K562	blood:
4	chr6:31619280..31620873-chr6:31935756..31938534,2	K562	blood:
5	chr6:31781426..31784987-chr6:31937458..31940746,3	K562	blood:
6	chr6:31628509..31634075-chr6:31935054..31938547,6	K562	blood:
7	chr6:31866210..31871385-chr6:31935988..31941288,8	K562	blood:
8	chr6:31631495..31634660-chr6:31935613..31943206,9	K562	blood:
9	chr6:31937366..31939733-chr6:32937181..32939543,3	K562	blood:
10	chr6:31701251..31705281-chr6:31936091..31940341,4	K562	blood:

No data

Variant related genes	Relation type
STK19	TF binding region
STK19	CpG island
ENSG00000204438	Chromatin interaction
ENSG00000204371	Chromatin interaction
ENSG00000204256	Chromatin interaction
ENSG00000204366	Chromatin interaction
ENSG00000204387	Chromatin interaction
ENSG00000204390	Chromatin interaction
ENSG00000263020	Chromatin interaction
ENSG00000204463	Chromatin interaction
ENSG00000201823	Chromatin interaction
ENSG00000201207	Chromatin interaction
ENSG00000204444	Chromatin interaction
ENSG00000166278	Chromatin interaction
ENSG00000204389	Chromatin interaction
ENSG00000204439	Chromatin interaction
ENSG00000212195	Chromatin interaction
ENSG00000213719	Chromatin interaction
ENSG00000204435	Chromatin interaction
ENSG00000223837	Chromatin interaction

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs2075701	0.81[ASN][1000 genomes]
rs2280773	0.81[ASN][1000 genomes]
rs4959020	0.81[ASN][1000 genomes]
rs4959082	0.81[ASN][1000 genomes]
rs57825471	0.87[ASN][1000 genomes]
rs60415038	0.83[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	nsv601610	chr6:31280101-31960770	Enhancers Flanking Active TSS Weak transcription Genic enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	370 gene(s)	inside rSNPs	diseases
2	nsv601628	chr6:31280327-31990098	Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	376 gene(s)	inside rSNPs	diseases
3	nsv601629	chr6:31280327-31996185	Strong transcription Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	376 gene(s)	inside rSNPs	diseases
4	nsv601630	chr6:31280327-32011317	Genic enhancers Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	378 gene(s)	inside rSNPs	diseases
5	nsv601631	chr6:31280327-32017540	Genic enhancers Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	378 gene(s)	inside rSNPs	diseases
6	nsv1023939	chr6:31325961-32026747	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	372 gene(s)	inside rSNPs	diseases
7	nsv538188	chr6:31325961-32026747	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	372 gene(s)	inside rSNPs	diseases
8	nsv1033154	chr6:31550614-32009410	Strong transcription Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	326 gene(s)	inside rSNPs	diseases
9	nsv1017945	chr6:31609641-32481240	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	322 gene(s)	inside rSNPs	diseases
10	nsv601950	chr6:31785438-32492308	Enhancers Bivalent Enhancer Active TSS Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	197 gene(s)	inside rSNPs	diseases
11	nsv601951	chr6:31785438-32496748	Enhancers Flanking Active TSS Strong transcription Weak transcription Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	197 gene(s)	inside rSNPs	diseases
12	nsv601955	chr6:31785453-32484368	Genic enhancers Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	196 gene(s)	inside rSNPs	diseases
13	nsv601956	chr6:31785453-32492308	Strong transcription Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	197 gene(s)	inside rSNPs	diseases
14	nsv601961	chr6:31868322-32484368	Enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	126 gene(s)	inside rSNPs	diseases
15	nsv427751	chr6:31871512-32092843	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	91 gene(s)	inside rSNPs	diseases
16	nsv428141	chr6:31871512-32092843	Enhancers Strong transcription Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	91 gene(s)	inside rSNPs	diseases
17	esv2758043	chr6:31871512-32209113	Genic enhancers Enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	114 gene(s)	inside rSNPs	diseases
18	esv2759415	chr6:31871512-32209113	Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	114 gene(s)	inside rSNPs	diseases
19	nsv830628	chr6:31887554-31947600	Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Genic enhancers Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	69 gene(s)	inside rSNPs	diseases
20	nsv933250	chr6:31905060-32008005	Weak transcription Genic enhancers Enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	76 gene(s)	inside rSNPs	diseases
21	nsv934279	chr6:31905060-32013902	Enhancers Flanking Active TSS Strong transcription Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
22	nsv884513	chr6:31922575-32066025	Bivalent Enhancer Strong transcription Weak transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	78 gene(s)	inside rSNPs	diseases
23	nsv884514	chr6:31923052-31958960	Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Weak transcription Active TSS Enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
24	nsv932869	chr6:31924496-32013902	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
25	nsv933913	chr6:31924682-32009282	Active TSS Strong transcription Weak transcription Genic enhancers Flanking Active TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
26	nsv284	chr6:31925739-31996721	Weak transcription Genic enhancers Active TSS Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
27	nsv5247	chr6:31925739-32023216	Transcr. at gene 5' and 3' Enhancers Genic enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
28	nsv884515	chr6:31930805-31946614	Active TSS Weak transcription Strong transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	51 gene(s)	inside rSNPs	diseases
29	nsv884516	chr6:31931673-31946614	Active TSS Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	51 gene(s)	inside rSNPs	diseases
30	nsv884517	chr6:31931673-32057627	Weak transcription Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
31	nsv538190	chr6:31932347-32037290	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
32	nsv884518	chr6:31933518-31946614	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	50 gene(s)	inside rSNPs	diseases
33	nsv884519	chr6:31937116-31947594	Enhancers Genic enhancers Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	49 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:31927400-31938800	Weak transcription	Right Atrium	heart
2	chr6:31927600-31939400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr6:31927800-31938400	Strong transcription	Lung	lung
4	chr6:31927800-31938600	Strong transcription	NHEK	skin
5	chr6:31928000-31937600	Strong transcription	Primary T killer memory cells from peripheral blood	blood
6	chr6:31928000-31937800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr6:31928000-31937800	Strong transcription	Brain Cingulate Gyrus	brain
8	chr6:31928000-31937800	Strong transcription	Brain Hippocampus Middle	brain
9	chr6:31928000-31937800	Strong transcription	Skeletal Muscle Male	skeletal muscle
10	chr6:31928000-31938000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr6:31928000-31938000	Strong transcription	Fetal Stomach	stomach
12	chr6:31928000-31938200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr6:31928000-31938200	Strong transcription	Fetal Intestine Small	intestine
14	chr6:31928000-31938200	Strong transcription	Fetal Muscle Trunk	muscle
15	chr6:31928000-31938200	Strong transcription	Placenta	Placenta
16	chr6:31928000-31938200	Strong transcription	Ovary	ovary
17	chr6:31928000-31938200	Strong transcription	Monocytes-CD14+_RO01746	blood
18	chr6:31928000-31938400	Strong transcription	HUES48 Cell Line	embryonic stem cell
19	chr6:31928000-31938400	Strong transcription	HUES6 Cell Line	embryonic stem cell
20	chr6:31928000-31938400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
21	chr6:31928000-31938400	Strong transcription	Primary neutrophils fromperipheralblood	blood
22	chr6:31928000-31938400	Strong transcription	Fetal Muscle Leg	muscle
23	chr6:31928000-31938600	Strong transcription	Rectal Smooth Muscle	rectum
24	chr6:31928000-31938600	Strong transcription	Sigmoid Colon	Sigmoid Colon
25	chr6:31928000-31938800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
26	chr6:31928200-31937600	Strong transcription	Duodenum Smooth Muscle	Duodenum
27	chr6:31928200-31937600	Strong transcription	NHLF	lung
28	chr6:31928200-31937800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr6:31928200-31937800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
30	chr6:31928200-31937800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr6:31928200-31937800	Strong transcription	Brain Angular Gyrus	brain
32	chr6:31928200-31937800	Strong transcription	Brain Substantia Nigra	brain
33	chr6:31928200-31937800	Strong transcription	Fetal Thymus	thymus
34	chr6:31928200-31937800	Strong transcription	Rectal Mucosa Donor 29	rectum
35	chr6:31928200-31937800	Strong transcription	Skeletal Muscle Female	skeletal muscle
36	chr6:31928200-31938000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr6:31928200-31938000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr6:31928200-31938000	Strong transcription	Adipose Nuclei	Adipose
39	chr6:31928200-31938000	Strong transcription	Brain Anterior Caudate	brain
40	chr6:31928200-31938200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr6:31928200-31938200	Strong transcription	Primary B cells from peripheral blood	blood
42	chr6:31928200-31938200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
43	chr6:31928200-31938200	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
44	chr6:31928200-31938200	Strong transcription	Colon Smooth Muscle	Colon
45	chr6:31928200-31938400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
46	chr6:31928200-31938400	Strong transcription	Primary monocytes fromperipheralblood	blood
47	chr6:31928200-31938400	Strong transcription	Primary B cells from cord blood	blood
48	chr6:31928200-31938400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
49	chr6:31928200-31938400	Strong transcription	Fetal Intestine Large	intestine
50	chr6:31928200-31938400	Strong transcription	Rectal Mucosa Donor 31	rectum

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