Variant report

Variant	rs3133658
Chromosome Location	chr8:95565538-95565539
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	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	ZNF143	chr8:95565397-95566223	K562	blood:	n/a	chr8:95565683-95565701
4	MAX	chr8:95565310-95566133	HepG2	liver:	n/a	n/a
5	CREB1	chr8:95565501-95566105	ECC-1	luminal epithelium:	n/a	n/a
6	POLR2A	chr8:95565255-95566387	K562	blood:	n/a	n/a
7	IRF1	chr8:95565469-95566421	K562	blood:	n/a	chr8:95565896-95565905 chr8:95565836-95565850
8	POLR2A	chr8:95565412-95566109	ECC-1	luminal epithelium:	n/a	n/a
9	MTA3	chr8:95565100-95566883	GM12878	blood:	n/a	n/a
10	POLR2A	chr8:95565340-95566855	GM12892	blood:	n/a	n/a
11	POLR2A	chr8:95565441-95565789	HepG2	liver:	n/a	n/a
12	MAX	chr8:95565384-95566598	ECC-1	luminal epithelium:	n/a	n/a
13	YY1	chr8:95565254-95566066	GM12891	blood:	n/a	chr8:95565665-95565685 chr8:95565667-95565679 chr8:95565859-95565873
14	ELF1	chr8:95565295-95566134	GM12878	blood:	n/a	chr8:95565705-95565716 chr8:95565706-95565715 chr8:95565704-95565717
15	NFIC	chr8:95565421-95566359	SK-N-SH	brain:	n/a	n/a
16	MEF2A	chr8:95565422-95566188	GM12878	blood:	n/a	chr8:95565425-95565433
17	POLR2A	chr8:95565396-95566135	HCT-116	colon:	n/a	n/a
18	POLR2A	chr8:95565300-95566765	HUVEC	blood vessel:	n/a	n/a
19	REST	chr8:95565309-95566534	HL-60	blood:	n/a	chr8:95565720-95565733
20	TAF1	chr8:95565436-95566163	Hela-S3	cervix:	n/a	n/a
21	POLR2A	chr8:95565460-95565779	GM12891	blood:	n/a	n/a
22	YY1	chr8:95565272-95566184	SK-N-SH_RA	brain:	n/a	chr8:95565665-95565685 chr8:95565667-95565679 chr8:95565859-95565873
23	NR2C2	chr8:95565446-95566058	HepG2	liver:	n/a	chr8:95565708-95565717 chr8:95565889-95565898
24	IRF1	chr8:95565518-95566477	K562	blood:	n/a	chr8:95565896-95565905 chr8:95565836-95565850
25	FOXA1	chr8:95565502-95566062	T-47D	breast:	n/a	n/a
26	YY1	chr8:95565194-95566082	K562	blood:	n/a	chr8:95565665-95565685 chr8:95565667-95565679 chr8:95565859-95565873
27	GATA3	chr8:95565422-95566226	MCF-7	breast:	n/a	chr8:95566111-95566122
28	SP4	chr8:95565515-95566168	H1-hESC	embryonic stem cell:	n/a	chr8:95565838-95565849 chr8:95566019-95566035
29	POLR2A	chr8:95565350-95566755	K562	blood:	n/a	n/a
30	CREB1	chr8:95565441-95566219	HepG2	liver:	n/a	n/a
31	GABPA	chr8:95565092-95566243	A549	lung:	n/a	chr8:95565683-95565692
32	RELA	chr8:95565422-95566393	GM19099	blood:	n/a	n/a
33	ELF1	chr8:95565465-95566059	HepG2	liver:	n/a	chr8:95565705-95565716 chr8:95565706-95565715 chr8:95565704-95565717
34	ATF2	chr8:95565524-95566160	GM12878	blood:	n/a	n/a
35	TAF1	chr8:95565473-95566116	GM12892	blood:	n/a	n/a
36	GATA3	chr8:95565247-95566358	MCF-7	breast:	n/a	chr8:95566111-95566122
37	GABPA	chr8:95564622-95566713	MCF-7	breast:	n/a	chr8:95565683-95565692
38	POLR2A	chr8:95565302-95566182	H1-neurons	neurons:	n/a	n/a
39	YY1	chr8:95565387-95566054	NT2-D1	testis:	n/a	chr8:95565665-95565685 chr8:95565667-95565679 chr8:95565859-95565873
40	PML	chr8:95565456-95566327	K562	blood:	n/a	n/a
41	NR2C2	chr8:95565307-95566056	Hela-S3	cervix:	n/a	chr8:95565708-95565717 chr8:95565889-95565898
42	CHD2	chr8:95565304-95566462	HepG2	liver:	n/a	n/a
43	RELA	chr8:95565278-95566403	GM10847	blood:	n/a	n/a
44	BCLAF1	chr8:95565349-95566233	GM12878	blood:	n/a	chr8:95565897-95565906 chr8:95565856-95565865
45	TCF12	chr8:95565063-95566573	A549	lung:	n/a	n/a
46	POLR2A	chr8:95565507-95566197	MCF-7	breast:	n/a	n/a
47	MEF2C	chr8:95565294-95566091	GM12878	blood:	n/a	chr8:95565425-95565433
48	POLR2A	chr8:95565172-95566275	PFSK-1	brain:	n/a	n/a
49	MXI1	chr8:95565342-95566183	Hela-S3	cervix:	n/a	n/a
50	TBP	chr8:95565469-95566171	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:95565502-95565552	HCPEpiC	choroid plexus:	n/a
2	chr8:95565502-95565552	HEEpiC	esophagus:	n/a
3	chr8:95565502-95565552	LNCaP	prostate:	n/a
4	chr8:95565502-95565552	Jurkat	blood:	n/a
5	chr8:95565502-95565552	RPTEC	kidney:	n/a
6	chr8:95565502-95565552	HRE	kidney:	n/a
7	chr8:95565502-95565552	CMK	blood:	n/a
8	chr8:95565502-95565552	HEK293	kidney:	embryo
9	chr8:95565502-95565552	HRPEpiC	eye:	n/a
10	chr8:95565502-95565552	GM06990	blood:	n/a
11	chr8:95565502-95565552	ProgFib	skin:	n/a
12	chr8:95565502-95565552	BJ	skin:	n/a
13	chr8:95565502-95565552	HPAEpiC	pulmonary alveolar:	n/a
14	chr8:95565502-95565552	AG04450	lung:	fetal
15	chr8:95565502-95565552	SAEC	small airway:	n/a
16	chr8:95565502-95565552	HRCEpiC	kidney:	n/a
17	chr8:95565502-95565552	K562	blood:	n/a
18	chr8:95565502-95565552	Hela-S3	cervix:	n/a
19	chr8:95565502-95565552	NB4	blood:	n/a
20	chr8:95565502-95565552	ECC-1	luminal epithelium:	n/a
21	chr8:95565502-95565552	AoSMC	blood vessel:	n/a
22	chr8:95565502-95565552	HAEpiC	amniotic membrane:	n/a
23	chr8:95565502-95565552	HL-60	blood:	n/a
24	chr8:95565502-95565552	SK-N-SH_RA	brain:	n/a
25	chr8:95565502-95565552	MCF-7	breast:	n/a
26	chr8:95565502-95565552	GM12892	blood:	n/a
27	chr8:95565502-95565552	MCF10A-Er-Src	breast:	n/a
28	chr8:95565502-95565552	SK-N-MC	brain:	n/a
29	chr8:95565502-95565552	PANC-1	pancreas:	n/a
30	chr8:95565502-95565552	HMEC	breast:	n/a
31	chr8:95565502-95565552	NT2-D1	testis:	n/a
32	chr8:95565502-95565552	H1-hESC	embryonic stem cell:	embryo
33	chr8:95565502-95565552	NHBE	bronchial:	n/a
34	chr8:95565502-95565552	A549	lung:	n/a
35	chr8:95565502-95565552	Caco-2	colon:	n/a
36	chr8:95565502-95565552	SKMC	muscle:	n/a
37	chr8:95565502-95565552	HCF	heart:	n/a
38	chr8:95565502-95565552	BE2_C	brain:	n/a
39	chr8:95565502-95565552	ovcar-3	ovarian:	n/a
40	chr8:95565502-95565552	NH-A	brain:	n/a
41	chr8:95565502-95565552	NHDF-neo	bronchial:	n/a
42	chr8:95565502-95565552	HNPCEpiC	eye:	n/a
43	chr8:95565502-95565552	GM12878	blood:	n/a
44	chr8:95565502-95565552	GM19239	blood:	n/a
45	chr8:95565502-95565552	AG04449	skin:	fetal
46	chr8:95565502-95565552	PFSK-1	brain:	n/a
47	chr8:95565502-95565552	Hepatocyte	liver:	n/a
48	chr8:95565502-95565552	U87	brain:	n/a
49	chr8:95565502-95565552	HIPEpiC	eye:	n/a
50	chr8:95565502-95565552	AG09319	gingival:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:39298720..39299544-chr8:95565528..95566062,2	Hela-S3	cervix:
2	chr8:95564422..95566417-chr8:95730460..95733624,3	K562	blood:
3	chr8:95564633..95567300-chr8:95651331..95653603,2	MCF-7	breast:
4	chr8:95564818..95567463-chr8:95729750..95733556,7	MCF-7	breast:
5	chr8:95564422..95566417-chr8:95731300..95733624,2	K562	blood:
6	chr8:95554974..95557880-chr8:95564950..95566849,3	MCF-7	breast:
7	chr8:95564312..95566828-chr8:95731001..95732970,2	MCF-7	breast:
8	chr8:95565366..95567177-chr8:96036825..96038672,2	K562	blood:
9	chr8:95563755..95566398-chr8:95651251..95655119,6	MCF-7	breast:

Variant related genes	Relation type
ENSG00000253704	TF binding region
ENSG00000253704	CpG island
ENSG00000139117	Chromatin interaction
ENSG00000261437	Chromatin interaction
ENSG00000164944	Chromatin interaction
ENSG00000156162	Chromatin interaction
ENSG00000156170	Chromatin interaction
ENSG00000104413	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[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1372047	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1834525	0.93[ASN][1000 genomes]
rs1866845	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2019783	0.81[JPT][hapmap]
rs2046666	1.00[CHB][hapmap];0.81[JPT][hapmap]
rs2099788	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2119460	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2246066	1.00[CHB][hapmap];0.82[JPT][hapmap]
rs2381830	0.89[AFR][1000 genomes];0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2381831	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2445721	1.00[CHB][hapmap];0.82[JPT][hapmap]
rs2450558	1.00[CHB][hapmap];0.82[JPT][hapmap]
rs2470739	1.00[CHB][hapmap];0.82[JPT][hapmap]
rs2470740	1.00[CHB][hapmap];0.82[JPT][hapmap]
rs2470742	1.00[CHB][hapmap];0.82[JPT][hapmap]
rs2515100	1.00[CHB][hapmap];0.81[JPT][hapmap]
rs2515153	1.00[CHB][hapmap]
rs2919654	1.00[CHB][hapmap];0.82[JPT][hapmap]
rs2921385	1.00[CHB][hapmap];0.81[JPT][hapmap]
rs2921387	1.00[CHB][hapmap];0.82[JPT][hapmap]
rs2930967	1.00[CHB][hapmap];0.81[JPT][hapmap]
rs2930969	1.00[CHB][hapmap];0.82[JPT][hapmap]
rs3098707	0.88[AFR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3098708	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.90[AFR][1000 genomes];0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3098709	0.88[AFR][1000 genomes];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3098712	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3098715	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs3098716	0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3098718	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3098719	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3098725	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs3099398	1.00[CHB][hapmap];0.87[JPT][hapmap]
rs3099403	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs3099404	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs3099406	0.80[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs3099407	0.96[CEU][hapmap];1.00[CHB][hapmap];0.81[JPT][hapmap];0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs3099412	0.96[CEU][hapmap];1.00[CHB][hapmap];0.81[JPT][hapmap];0.83[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs3099413	0.80[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs3102841	1.00[CHB][hapmap];0.83[AMR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs3102845	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs3102847	0.85[ASN][1000 genomes]
rs3102851	0.91[ASN][1000 genomes]
rs3102855	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs3102859	0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3102862	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs3102874	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3102875	0.92[AMR][1000 genomes];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs3102877	0.88[AFR][1000 genomes];0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3133601	0.93[ASN][1000 genomes]
rs3133635	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs3133637	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs3133640	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs3133645	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3133648	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3133649	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3133651	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3133654	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];0.91[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3133656	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];0.89[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3133657	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	0.86[CEU][hapmap]
rs935052	1.00[CHB][hapmap];0.81[JPT][hapmap]
rs957446	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[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	chr8:95564200-95566600	Active TSS	Fetal Muscle Leg	muscle
4	chr8:95564200-95566800	Active TSS	iPS-18 Cell Line	embryonic stem cell
5	chr8:95564200-95567000	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr8:95564200-95567000	Active TSS	HUES64 Cell Line	embryonic stem cell
7	chr8:95564200-95567000	Active TSS	iPS-15b Cell Line	embryonic stem cell
8	chr8:95564200-95567200	Active TSS	HMEC	breast
9	chr8:95564200-95567200	Active TSS	K562	blood
10	chr8:95564400-95566800	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr8:95564400-95567000	Active TSS	HUES48 Cell Line	embryonic stem cell
12	chr8:95564400-95567000	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr8:95564400-95567000	Active TSS	iPS-20b Cell Line	embryonic stem cell
14	chr8:95564400-95567000	Active TSS	Aorta	Aorta
15	chr8:95564400-95567000	Active TSS	Fetal Intestine Large	intestine
16	chr8:95564400-95567000	Active TSS	Right Atrium	heart
17	chr8:95564400-95567200	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr8:95564400-95567200	Active TSS	NHLF	lung
19	chr8:95564600-95565600	Flanking Active TSS	Adipose Nuclei	Adipose
20	chr8:95564600-95566800	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr8:95564600-95566800	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
22	chr8:95564600-95566800	Active TSS	Breast Myoepithelial Primary Cells	Breast
23	chr8:95564600-95567000	Active TSS	H1 Cell Line	embryonic stem cell
24	chr8:95564600-95567000	Active TSS	Fetal Kidney	kidney
25	chr8:95564600-95567000	Active TSS	HSMMtube	muscle
26	chr8:95564600-95567200	Active TSS	Muscle Satellite Cultured Cells	--
27	chr8:95564600-95567200	Active TSS	A549	lung
28	chr8:95564600-95567200	Active TSS	NHDF-Ad	bronchial
29	chr8:95564600-95567400	Active TSS	GM12878-XiMat	blood
30	chr8:95564800-95565600	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
31	chr8:95564800-95565600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
32	chr8:95564800-95566600	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
33	chr8:95564800-95566600	Active TSS	Fetal Heart	heart
34	chr8:95564800-95566600	Active TSS	Fetal Muscle Trunk	muscle
35	chr8:95564800-95566600	Active TSS	Placenta	Placenta
36	chr8:95564800-95566600	Active TSS	Hela-S3	cervix
37	chr8:95564800-95566800	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr8:95564800-95566800	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr8:95564800-95566800	Active TSS	Brain Substantia Nigra	brain
40	chr8:95564800-95566800	Active TSS	Left Ventricle	heart
41	chr8:95564800-95566800	Active TSS	Thymus	Thymus
42	chr8:95564800-95567000	Active TSS	ES-I3 Cell Line	embryonic stem cell
43	chr8:95564800-95567000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
44	chr8:95564800-95567000	Active TSS	H9 Cell Line	embryonic stem cell
45	chr8:95564800-95567000	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr8:95564800-95567000	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
47	chr8:95564800-95567000	Active TSS	Brain Hippocampus Middle	brain
48	chr8:95564800-95567000	Active TSS	Esophagus	oesophagus
49	chr8:95564800-95567000	Active TSS	Ovary	ovary
50	chr8:95564800-95567000	Active TSS	Placenta Amnion	Placenta Amnion

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