Variant report

Variant	rs3133657
Chromosome Location	chr8:95565273-95565274
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ELF1	chr8:95565161-95566155	MCF-7	breast:	n/a	chr8:95565705-95565716 chr8:95565706-95565715 chr8:95565704-95565717
2	NFIC	chr8:95564979-95566501	GM12878	blood:	n/a	n/a
3	POLR2A	chr8:95565255-95566387	K562	blood:	n/a	n/a
4	MTA3	chr8:95565100-95566883	GM12878	blood:	n/a	n/a
5	YY1	chr8:95565254-95566066	GM12891	blood:	n/a	chr8:95565665-95565685 chr8:95565667-95565679 chr8:95565859-95565873
6	YY1	chr8:95565272-95566184	SK-N-SH_RA	brain:	n/a	chr8:95565665-95565685 chr8:95565667-95565679 chr8:95565859-95565873
7	YY1	chr8:95565194-95566082	K562	blood:	n/a	chr8:95565665-95565685 chr8:95565667-95565679 chr8:95565859-95565873
8	GABPA	chr8:95565092-95566243	A549	lung:	n/a	chr8:95565683-95565692
9	GATA3	chr8:95565247-95566358	MCF-7	breast:	n/a	chr8:95566111-95566122
10	GABPA	chr8:95564622-95566713	MCF-7	breast:	n/a	chr8:95565683-95565692
11	TCF12	chr8:95565063-95566573	A549	lung:	n/a	n/a
12	POLR2A	chr8:95565172-95566275	PFSK-1	brain:	n/a	n/a
13	SP1	chr8:95565094-95566392	HCT-116	colon:	n/a	chr8:95565838-95565849 chr8:95566014-95566028
14	MXI1	chr8:95565073-95566146	H1-hESC	embryonic stem cell:	n/a	n/a
15	REST	chr8:95565257-95566380	A549	lung:	n/a	chr8:95565720-95565733
16	REST	chr8:95564985-95566553	H1-neurons	neurons:	n/a	chr8:95565720-95565733
17	MAZ	chr8:95565181-95566410	K562	blood:	n/a	n/a
18	POLR2A	chr8:95565262-95566523	ProgFib	skin:	n/a	n/a
19	POLR2A	chr8:95565022-95566820	GM12878	blood:	n/a	n/a
20	YY1	chr8:95565106-95566166	HCT-116	colon:	n/a	chr8:95565665-95565685 chr8:95565667-95565679 chr8:95565859-95565873
21	GABPA	chr8:95565056-95566511	SK-N-SH	brain:	n/a	chr8:95565683-95565692
22	GABPA	chr8:95564964-95566397	A549	lung:	n/a	chr8:95565683-95565692
23	RELA	chr8:95565251-95566695	GM15510	blood:	n/a	n/a
24	TAF1	chr8:95565184-95566327	A549	lung:	n/a	n/a
25	EP300	chr8:95565254-95566245	A549	lung:	n/a	chr8:95565706-95565713 chr8:95565766-95565773
26	WRNIP1	chr8:95564949-95566423	GM12878	blood:	n/a	n/a
27	SIN3AK20	chr8:95565066-95566638	MCF-7	breast:	n/a	n/a
28	GATA1	chr8:95565220-95566930	PBDE	blood:	n/a	chr8:95566111-95566122
29	SIN3AK20	chr8:95565186-95566203	PANC-1	pancreas:	n/a	n/a
30	TAF1	chr8:95565231-95566170	H1-neurons	neurons:	n/a	n/a
31	GABPA	chr8:95565007-95566247	MCF-7	breast:	n/a	chr8:95565683-95565692
32	POLR2A	chr8:95565190-95566816	GM12891	blood:	n/a	n/a
33	SP1	chr8:95565247-95566318	A549	lung:	n/a	chr8:95565838-95565849 chr8:95566014-95566028
34	HCFC1	chr8:95565108-95566332	K562	blood:	n/a	n/a
35	POLR2A	chr8:95565165-95566602	MCF10A-Er-Src	breast:	n/a	n/a
36	TAF1	chr8:95565187-95566221	K562	blood:	n/a	n/a
37	SIN3AK20	chr8:95565126-95565747	H1-hESC	embryonic stem cell:	n/a	n/a
38	RUNX3	chr8:95565189-95566222	GM12878	blood:	n/a	n/a
39	IRF1	chr8:95565019-95566860	K562	blood:	n/a	chr8:95565095-95565102 chr8:95565896-95565905 chr8:95565836-95565850
40	YY1	chr8:95564980-95566418	SK-N-SH	brain:	n/a	chr8:95565665-95565685 chr8:95565667-95565679 chr8:95565859-95565873
41	MAX	chr8:95565233-95566878	A549	lung:	n/a	n/a
42	SIN3A	chr8:95565019-95566439	H1-hESC	embryonic stem cell:	n/a	chr8:95565856-95565867
43	YY1	chr8:95565257-95566016	GM12892	blood:	n/a	chr8:95565665-95565685 chr8:95565667-95565679 chr8:95565859-95565873
44	POLR2A	chr8:95565147-95566440	PFSK-1	brain:	n/a	n/a
45	YY1	chr8:95565160-95566142	GM12878	blood:	n/a	chr8:95565665-95565685 chr8:95565667-95565679 chr8:95565859-95565873
46	YY1	chr8:95565231-95566082	HepG2	liver:	n/a	chr8:95565665-95565685 chr8:95565667-95565679 chr8:95565859-95565873
47	MAX	chr8:95565255-95566135	K562	blood:	n/a	n/a
48	SIN3AK20	chr8:95565018-95566914	MCF-7	breast:	n/a	n/a
49	POLR2A	chr8:95565008-95567007	SK-N-MC	brain:	n/a	n/a
50	HCFC1	chr8:95564625-95566480	Hela-S3	cervix:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:95565249-95565299	HRE	kidney:	n/a
2	chr8:95565249-95565299	NHBE	bronchial:	n/a
3	chr8:95565249-95565299	LNCaP	prostate:	n/a
4	chr8:95565249-95565299	AG10803	skin:	n/a
5	chr8:95565249-95565299	GM12878	blood:	n/a
6	chr8:95565249-95565299	HNPCEpiC	eye:	n/a
7	chr8:95565249-95565299	HIPEpiC	eye:	n/a
8	chr8:95565249-95565299	HEEpiC	esophagus:	n/a
9	chr8:95565249-95565299	Jurkat	blood:	n/a
10	chr8:95565249-95565299	HMEC	breast:	n/a
11	chr8:95565249-95565299	PFSK-1	brain:	n/a
12	chr8:95565249-95565299	Hela-S3	cervix:	n/a
13	chr8:95565249-95565299	PrEC	prostate:	n/a
14	chr8:95565249-95565299	MCF10A-Er-Src	breast:	n/a
15	chr8:95565249-95565299	NB4	blood:	n/a
16	chr8:95565249-95565299	H1-hESC	embryonic stem cell:	embryo
17	chr8:95565249-95565299	HRCEpiC	kidney:	n/a
18	chr8:95565249-95565299	NT2-D1	testis:	n/a
19	chr8:95565249-95565299	HAEpiC	amniotic membrane:	n/a
20	chr8:95565249-95565299	HEK293	kidney:	embryo
21	chr8:95565249-95565299	SK-N-SH_RA	brain:	n/a
22	chr8:95565249-95565299	AG09319	gingival:	n/a
23	chr8:95565249-95565299	A549	lung:	n/a
24	chr8:95565249-95565299	ProgFib	skin:	n/a
25	chr8:95565249-95565299	HPAEpiC	pulmonary alveolar:	n/a
26	chr8:95565249-95565299	IMR90	lung:	fetal
27	chr8:95565249-95565299	ovcar-3	ovarian:	n/a
28	chr8:95565249-95565299	CMK	blood:	n/a
29	chr8:95565249-95565299	MCF-7	breast:	n/a
30	chr8:95565249-95565299	U87	brain:	n/a
31	chr8:95565249-95565299	HL-60	blood:	n/a
32	chr8:95565249-95565299	BJ	skin:	n/a
33	chr8:95565249-95565299	Hepatocyte	liver:	n/a
34	chr8:95565249-95565299	AG09309	skin:	n/a
35	chr8:95565249-95565299	HCF	heart:	n/a
36	chr8:95565249-95565299	AG04449	skin:	fetal
37	chr8:95565249-95565299	HCT-116	colon:	n/a
38	chr8:95565249-95565299	NH-A	brain:	n/a
39	chr8:95565249-95565299	GM19239	blood:	n/a
40	chr8:95565249-95565299	K562	blood:	n/a
41	chr8:95565249-95565299	AG04450	lung:	fetal
42	chr8:95565249-95565299	SAEC	small airway:	n/a
43	chr8:95565249-95565299	NHDF-neo	bronchial:	n/a
44	chr8:95565249-95565299	RPTEC	kidney:	n/a
45	chr8:95565249-95565299	GM12892	blood:	n/a
46	chr8:95565249-95565299	HepG2	liver:	n/a
47	chr8:95565249-95565299	HRPEpiC	eye:	n/a
48	chr8:95565249-95565299	T-47D	breast:	n/a
49	chr8:95565249-95565299	HUVEC	blood vessel:	n/a
50	chr8:95565249-95565299	SK-N-SH	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:95564422..95566417-chr8:95730460..95733624,3	K562	blood:
2	chr8:95564633..95567300-chr8:95651331..95653603,2	MCF-7	breast:
3	chr8:95564818..95567463-chr8:95729750..95733556,7	MCF-7	breast:
4	chr8:95564422..95566417-chr8:95731300..95733624,2	K562	blood:
5	chr8:95554974..95557880-chr8:95564950..95566849,3	MCF-7	breast:
6	chr8:95564312..95566828-chr8:95731001..95732970,2	MCF-7	breast:
7	chr8:95563755..95566398-chr8:95651251..95655119,6	MCF-7	breast:

Variant related genes	Relation type
ENSG00000253704	TF binding region
ENSG00000253704	CpG island
ENSG00000261437	Chromatin interaction
ENSG00000164944	Chromatin interaction
ENSG00000104413	Chromatin interaction
ENSG00000156162	Chromatin interaction

Extended variants
information (count: 79 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:63)

rs_ID	r²[population]
rs1023766	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.96[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.98[LWK][hapmap];1.00[MEX][hapmap];0.92[MKK][hapmap];1.00[TSI][hapmap];0.86[YRI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1372047	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1834525	0.93[ASN][1000 genomes]
rs1866845	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2019783	0.85[CHD][hapmap];0.81[JPT][hapmap]
rs2046666	1.00[CHB][hapmap];0.81[JPT][hapmap]
rs2099788	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2119460	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2246066	1.00[CHB][hapmap];0.81[JPT][hapmap]
rs2381830	0.94[AFR][1000 genomes];0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2381831	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2445721	1.00[CHB][hapmap];0.81[JPT][hapmap]
rs2450558	1.00[CHB][hapmap];0.81[JPT][hapmap]
rs2470739	1.00[CHB][hapmap];0.81[JPT][hapmap]
rs2470740	1.00[CHB][hapmap];0.81[JPT][hapmap]
rs2470742	1.00[CHB][hapmap];0.81[JPT][hapmap]
rs2515100	1.00[CHB][hapmap];0.81[JPT][hapmap]
rs2515153	1.00[CHB][hapmap];0.81[CHD][hapmap]
rs2919654	1.00[CHB][hapmap];0.81[JPT][hapmap]
rs2921385	1.00[CHB][hapmap];0.81[JPT][hapmap]
rs2921387	1.00[CHB][hapmap];0.81[JPT][hapmap]
rs2930967	1.00[CHB][hapmap];0.84[CHD][hapmap];0.81[JPT][hapmap]
rs2930969	1.00[CHB][hapmap];0.81[JPT][hapmap]
rs3098707	0.93[AFR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3098708	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3098709	0.92[AFR][1000 genomes];0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3098712	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.96[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.82[LWK][hapmap];1.00[MEX][hapmap];0.85[MKK][hapmap];1.00[TSI][hapmap];0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3098715	0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs3098716	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3098718	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3098719	0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3098725	1.00[CEU][hapmap];1.00[CHB][hapmap];0.96[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap];1.00[TSI][hapmap];0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs3099398	1.00[CHB][hapmap];0.93[CHD][hapmap];0.87[JPT][hapmap]
rs3099403	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs3099404	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs3099406	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs3099407	0.96[CEU][hapmap];1.00[CHB][hapmap];0.85[CHD][hapmap];0.93[GIH][hapmap];0.81[JPT][hapmap];0.88[MEX][hapmap];0.91[TSI][hapmap];0.82[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs3099412	0.96[CEU][hapmap];1.00[CHB][hapmap];0.85[CHD][hapmap];0.93[GIH][hapmap];0.81[JPT][hapmap];0.88[MEX][hapmap];0.91[TSI][hapmap];0.81[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs3099413	0.86[EUR][1000 genomes]
rs3102841	0.81[ASW][hapmap];1.00[CHB][hapmap];0.93[CHD][hapmap];0.84[GIH][hapmap];0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs3102845	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs3102847	0.85[ASN][1000 genomes]
rs3102851	0.91[ASN][1000 genomes]
rs3102855	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs3102859	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3102862	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs3102874	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3102875	0.90[AMR][1000 genomes];0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs3102877	0.92[AFR][1000 genomes];0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3133601	0.93[ASN][1000 genomes]
rs3133635	0.83[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs3133637	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs3133640	0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs3133645	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3133648	0.88[ASW][hapmap];1.00[CHB][hapmap];0.96[CHD][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];0.93[LWK][hapmap];0.94[MEX][hapmap];0.88[MKK][hapmap];0.93[TSI][hapmap];0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3133649	0.83[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3133651	1.00[CEU][hapmap];1.00[CHB][hapmap];0.96[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.81[LWK][hapmap];1.00[MEX][hapmap];0.88[MKK][hapmap];1.00[TSI][hapmap];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3133654	0.87[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.96[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3133656	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.96[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.98[LWK][hapmap];1.00[MEX][hapmap];0.92[MKK][hapmap];1.00[TSI][hapmap];0.86[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3133658	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4734279	0.85[CEU][hapmap]
rs935052	1.00[CHB][hapmap];0.81[JPT][hapmap]
rs957446	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1017301	chr8:95273503-96248352	Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
2	nsv539680	chr8:95273503-96248352	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
3	nsv532338	chr8:95296118-95971825	Enhancers Strong transcription Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised 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
4	nsv429928	chr8:95488800-95672033	Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
5	nsv611750	chr8:95519205-95574634	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Genic 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	13 gene(s)	inside rSNPs	diseases
6	nsv1017256	chr8:95555083-95570079	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
7	nsv1026768	chr8:95556054-95569566	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
8	nsv1033318	chr8:95556054-95576338	Flanking Active TSS Strong transcription Active TSS Enhancers Weak transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
9	nsv1032065	chr8:95556054-95578349	Active TSS Weak transcription Flanking Active TSS Enhancers Genic enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
10	nsv1016339	chr8:95556054-95585807	Strong transcription Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
11	nsv1021702	chr8:95556054-95589194	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
12	nsv1033345	chr8:95556375-95570533	Active TSS Strong transcription Weak transcription Flanking Active TSS Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
13	nsv1029802	chr8:95556959-95578349	Flanking Active TSS Weak transcription Strong transcription Active TSS Enhancers Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
14	esv3584580	chr8:95557287-95576350	Weak transcription Active TSS Enhancers Genic enhancers Flanking Active TSS 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 lncRNA	10 gene(s)	inside rSNPs	diseases
15	nsv438072	chr8:95558694-95571443	Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Bivalent/Poised TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
16	nsv429929	chr8:95564533-95676894	Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Strong transcription Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:95563400-95566800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr8:95564000-95567000	Active TSS	HUES6 Cell Line	embryonic stem cell
3	chr8:95564200-95565400	Flanking Active TSS	Duodenum Mucosa	Duodenum
4	chr8:95564200-95566600	Active TSS	Fetal Muscle Leg	muscle
5	chr8:95564200-95566800	Active TSS	iPS-18 Cell Line	embryonic stem cell
6	chr8:95564200-95567000	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr8:95564200-95567000	Active TSS	HUES64 Cell Line	embryonic stem cell
8	chr8:95564200-95567000	Active TSS	iPS-15b Cell Line	embryonic stem cell
9	chr8:95564200-95567200	Active TSS	HMEC	breast
10	chr8:95564200-95567200	Active TSS	K562	blood
11	chr8:95564400-95565400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
12	chr8:95564400-95566800	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr8:95564400-95567000	Active TSS	HUES48 Cell Line	embryonic stem cell
14	chr8:95564400-95567000	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr8:95564400-95567000	Active TSS	iPS-20b Cell Line	embryonic stem cell
16	chr8:95564400-95567000	Active TSS	Aorta	Aorta
17	chr8:95564400-95567000	Active TSS	Fetal Intestine Large	intestine
18	chr8:95564400-95567000	Active TSS	Right Atrium	heart
19	chr8:95564400-95567200	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr8:95564400-95567200	Active TSS	NHLF	lung
21	chr8:95564600-95565400	Flanking Active TSS	Primary B cells from cord blood	blood
22	chr8:95564600-95565400	Flanking Active TSS	Primary T cells from cord blood	blood
23	chr8:95564600-95565400	Flanking Active TSS	Primary hematopoietic stem cells	blood
24	chr8:95564600-95565400	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
25	chr8:95564600-95565400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr8:95564600-95565400	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
27	chr8:95564600-95565400	Flanking Active TSS	Rectal Smooth Muscle	rectum
28	chr8:95564600-95565600	Flanking Active TSS	Adipose Nuclei	Adipose
29	chr8:95564600-95566800	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr8:95564600-95566800	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
31	chr8:95564600-95566800	Active TSS	Breast Myoepithelial Primary Cells	Breast
32	chr8:95564600-95567000	Active TSS	H1 Cell Line	embryonic stem cell
33	chr8:95564600-95567000	Active TSS	Fetal Kidney	kidney
34	chr8:95564600-95567000	Active TSS	HSMMtube	muscle
35	chr8:95564600-95567200	Active TSS	Muscle Satellite Cultured Cells	--
36	chr8:95564600-95567200	Active TSS	A549	lung
37	chr8:95564600-95567200	Active TSS	NHDF-Ad	bronchial
38	chr8:95564600-95567400	Active TSS	GM12878-XiMat	blood
39	chr8:95564800-95565400	Flanking Active TSS	Primary B cells from peripheral blood	blood
40	chr8:95564800-95565400	Flanking Active TSS	Primary T cells fromperipheralblood	blood
41	chr8:95564800-95565400	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
42	chr8:95564800-95565400	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
43	chr8:95564800-95565400	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
44	chr8:95564800-95565600	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
45	chr8:95564800-95565600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
46	chr8:95564800-95566600	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
47	chr8:95564800-95566600	Active TSS	Fetal Heart	heart
48	chr8:95564800-95566600	Active TSS	Fetal Muscle Trunk	muscle
49	chr8:95564800-95566600	Active TSS	Placenta	Placenta
50	chr8:95564800-95566600	Active TSS	Hela-S3	cervix

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