Variant report

Variant	rs1687032
Chromosome Location	chr12:34175126-34175127
allele	A/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	MAX	chr12:34175070-34175478	HepG2	liver:	n/a	n/a
2	MAX	chr12:34175040-34175541	GM12878	blood:	n/a	n/a
3	CTCF	chr12:34174898-34175296	T-47D	breast:	n/a	chr12:34175123-34175141 chr12:34175124-34175140 chr12:34175118-34175139
4	MAX	chr12:34175079-34175465	H1-hESC	embryonic stem cell:	n/a	n/a
5	STAT5A	chr12:34174878-34175595	K562	blood:	n/a	n/a
6	STAT5A	chr12:34175101-34175608	GM12878	blood:	n/a	n/a
7	CTCF	chr12:34175060-34175210	AG09309	skin:	n/a	chr12:34175123-34175141 chr12:34175124-34175140 chr12:34175118-34175139
8	USF1	chr12:34175079-34175581	A549	lung:	n/a	n/a
9	IRF1	chr12:34175040-34175585	K562	blood:	n/a	chr12:34175100-34175117
10	GABPA	chr12:34175009-34175597	SK-N-SH	brain:	n/a	n/a
11	MYC	chr12:34175060-34175552	K562	blood:	n/a	n/a
12	CTCF	chr12:34175040-34175190	NHDF-neo	bronchial:	n/a	chr12:34175123-34175141 chr12:34175124-34175140 chr12:34175118-34175139
13	POLR2A	chr12:34175033-34175996	GM15510	blood:	n/a	n/a
14	CTCF	chr12:34175035-34175264	GM13977	blood:	n/a	chr12:34175123-34175141 chr12:34175124-34175140 chr12:34175118-34175139
15	CTCF	chr12:34175022-34175224	NHEK	skin:	n/a	chr12:34175123-34175141 chr12:34175124-34175140 chr12:34175118-34175139
16	MEF2A	chr12:34174864-34175467	GM12878	blood:	n/a	n/a
17	MAX	chr12:34175052-34175569	NB4	blood:	n/a	n/a
18	FOXA1	chr12:34174862-34175544	HepG2	liver:	n/a	chr12:34174865-34174877
19	SP1	chr12:34174942-34175577	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr12:34175040-34175190	AG04450	lung:	n/a	chr12:34175123-34175141 chr12:34175124-34175140 chr12:34175118-34175139
21	CTCF	chr12:34175020-34175170	GM12870	blood:	n/a	chr12:34175123-34175141 chr12:34175124-34175140 chr12:34175118-34175139
22	CTCF	chr12:34175060-34175210	HMEC	breast:	n/a	chr12:34175123-34175141 chr12:34175124-34175140 chr12:34175118-34175139
23	SMC3	chr12:34174884-34175481	HepG2	liver:	n/a	chr12:34175125-34175139
24	CTCF	chr12:34175060-34175210	AG10803	skin:	n/a	chr12:34175123-34175141 chr12:34175124-34175140 chr12:34175118-34175139
25	STAT3	chr12:34175067-34175524	MCF10A-Er-Src	breast:	n/a	n/a
26	CTCF	chr12:34175068-34175412	MCF-7	breast:	n/a	chr12:34175123-34175141 chr12:34175124-34175140 chr12:34175118-34175139
27	GABPA	chr12:34174771-34176031	MCF-7	breast:	n/a	n/a
28	CTCF	chr12:34174993-34175286	Pancreas_OC	pancreas:	n/a	chr12:34175123-34175141 chr12:34175124-34175140 chr12:34175118-34175139
29	CTCF	chr12:34175040-34175190	HVMF	connective:	n/a	chr12:34175123-34175141 chr12:34175124-34175140 chr12:34175118-34175139
30	MEF2C	chr12:34175061-34175561	GM12878	blood:	n/a	n/a
31	POLR2A	chr12:34175067-34175813	U87	brain:	n/a	n/a
32	HCFC1	chr12:34174804-34175823	Hela-S3	cervix:	n/a	n/a
33	CTCF	chr12:34175060-34175210	HRPEpiC	eye:	n/a	chr12:34175123-34175141 chr12:34175124-34175140 chr12:34175118-34175139
34	CTCF	chr12:34175020-34175170	HFF-Myc	foreskin:	n/a	chr12:34175123-34175141 chr12:34175124-34175140 chr12:34175118-34175139
35	CEBPB	chr12:34175041-34175483	A549	lung:	n/a	n/a
36	KAP1	chr12:34175043-34175656	HEK293	kidney:	n/a	n/a
37	RAD21	chr12:34174939-34175380	MCF-7	breast:	n/a	chr12:34175121-34175140
38	CREB1	chr12:34175118-34175426	A549	lung:	n/a	n/a
39	PML	chr12:34174845-34175766	GM12878	blood:	n/a	n/a
40	CTCF	chr12:34174629-34175629	SK-N-SH	brain:	n/a	chr12:34175123-34175141 chr12:34175124-34175140 chr12:34175118-34175139
41	ATF2	chr12:34174909-34175573	GM12878	blood:	n/a	n/a
42	POLR2A	chr12:34174935-34175680	SK-N-SH	brain:	n/a	n/a
43	KAP1	chr12:34174970-34175645	U2OS	brain:	n/a	n/a
44	REST	chr12:34175043-34175730	A549	lung:	n/a	n/a
45	CTCF	chr12:34175100-34175250	GM12867	blood:	n/a	chr12:34175123-34175141 chr12:34175124-34175140 chr12:34175118-34175139
46	MYBL2	chr12:34175022-34175631	HepG2	liver:	n/a	n/a
47	STAT3	chr12:34175084-34175534	MCF10A-Er-Src	breast:	n/a	n/a
48	ZNF143	chr12:34175053-34175592	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTCF	chr12:34175043-34175244	GM20000	blood:	n/a	chr12:34175123-34175141 chr12:34175124-34175140 chr12:34175118-34175139
50	ELF1	chr12:34175075-34175602	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:34175126-34175176	HCM	heart:	n/a
2	chr12:34175126-34175176	BE2_C	brain:	n/a
3	chr12:34175126-34175176	AG04449	skin:	fetal
4	chr12:34175126-34175176	AG10803	skin:	n/a
5	chr12:34175126-34175176	SAEC	small airway:	n/a
6	chr12:34175126-34175176	A549	lung:	n/a
7	chr12:34175126-34175176	HEK293	kidney:	embryo
8	chr12:34175126-34175176	HRCEpiC	kidney:	n/a
9	chr12:34175126-34175176	HL-60	blood:	n/a
10	chr12:34175126-34175176	HAEpiC	amniotic membrane:	n/a
11	chr12:34175126-34175176	NHBE	bronchial:	n/a
12	chr12:34175126-34175176	HCF	heart:	n/a
13	chr12:34175126-34175176	AG09319	gingival:	n/a
14	chr12:34175126-34175176	SK-N-MC	brain:	n/a
15	chr12:34175126-34175176	GM19239	blood:	n/a
16	chr12:34175126-34175176	NH-A	brain:	n/a
17	chr12:34175126-34175176	HIPEpiC	eye:	n/a
18	chr12:34175126-34175176	NHDF-neo	bronchial:	n/a
19	chr12:34175126-34175176	HCPEpiC	choroid plexus:	n/a
20	chr12:34175126-34175176	PANC-1	pancreas:	n/a
21	chr12:34175126-34175176	HCT-116	colon:	n/a
22	chr12:34175126-34175176	Caco-2	colon:	n/a
23	chr12:34175126-34175176	GM12892	blood:	n/a
24	chr12:34175126-34175176	Jurkat	blood:	n/a
25	chr12:34175126-34175176	ovcar-3	ovarian:	n/a
26	chr12:34175126-34175176	AG04450	lung:	fetal
27	chr12:34175126-34175176	RPTEC	kidney:	n/a
28	chr12:34175126-34175176	ECC-1	luminal epithelium:	n/a
29	chr12:34175126-34175176	H1-hESC	embryonic stem cell:	embryo
30	chr12:34175126-34175176	IMR90	lung:	fetal
31	chr12:34175126-34175176	AG09309	skin:	n/a
32	chr12:34175126-34175176	MCF10A-Er-Src	breast:	n/a
33	chr12:34175126-34175176	PrEC	prostate:	n/a
34	chr12:34175126-34175176	T-47D	breast:	n/a
35	chr12:34175126-34175176	GM12891	blood:	n/a
36	chr12:34175126-34175176	Hepatocyte	liver:	n/a
37	chr12:34175126-34175176	HMEC	breast:	n/a
38	chr12:34175126-34175176	GM06990	blood:	n/a
39	chr12:34175126-34175176	HUVEC	blood vessel:	n/a
40	chr12:34175126-34175176	CMK	blood:	n/a
41	chr12:34175126-34175176	HRPEpiC	eye:	n/a
42	chr12:34175126-34175176	HepG2	liver:	n/a
43	chr12:34175126-34175176	LNCaP	prostate:	n/a
44	chr12:34175126-34175176	BJ	skin:	n/a
45	chr12:34175126-34175176	MCF-7	breast:	n/a
46	chr12:34175126-34175176	U87	brain:	n/a
47	chr12:34175126-34175176	HRE	kidney:	n/a
48	chr12:34175126-34175176	SK-N-SH	brain:	n/a
49	chr12:34175126-34175176	NB4	blood:	n/a
50	chr12:34175126-34175176	NT2-D1	testis:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:32908405..32909605-chr12:34174701..34175708,3	MCF-7	breast:
2	chr12:34175001..34175865-chr12:38710413..38711151,3	HCT-116	colon:

Variant related genes	Relation type
ALG10	TF binding region
ALG10	CpG island
ENSG00000175548	Chromatin interaction
ENSG00000139131	Chromatin interaction

Extended variants
information (count: 78 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs11830127	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11831435	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11832550	1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs11835762	0.93[EUR][1000 genomes]
rs11838072	0.80[AFR][1000 genomes]
rs1687029	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1687035	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1705760	1.00[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1968959	1.00[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs304312	1.00[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs433479	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs55742885	1.00[ASN][1000 genomes]
rs57871101	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60104166	0.81[EUR][1000 genomes]
rs638101	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs667452	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs674968	0.85[EUR][1000 genomes]
rs67696537	1.00[ASN][1000 genomes]
rs7297954	0.81[EUR][1000 genomes]
rs7308325	0.81[EUR][1000 genomes]
rs73096217	0.81[EUR][1000 genomes]
rs73096221	0.81[EUR][1000 genomes]
rs73096248	0.81[EUR][1000 genomes]
rs73096255	0.81[EUR][1000 genomes]
rs73096278	0.81[EUR][1000 genomes]
rs74073506	0.93[EUR][1000 genomes]
rs74073512	0.93[EUR][1000 genomes]
rs74073536	1.00[ASN][1000 genomes]
rs74075710	0.80[AFR][1000 genomes]
rs74075717	0.80[AFR][1000 genomes]
rs74075723	1.00[AMR][1000 genomes]
rs74075737	1.00[AMR][1000 genomes]
rs74075754	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs74075755	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7964221	1.00[ASN][1000 genomes]
rs814660	1.00[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs814662	1.00[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs923533	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:40 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv558247	chr12:33481504-34245756	Weak transcription Flanking Bivalent TSS/Enh Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
2	nsv1037735	chr12:33510115-34457196	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
3	nsv469348	chr12:33524082-34245756	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
4	nsv558249	chr12:33524082-34245756	Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
5	nsv1047430	chr12:33526355-34435009	Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
6	nsv1040037	chr12:33526355-34457196	Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
7	nsv1049273	chr12:33528203-34491300	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Active TSS Weak transcription Enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
8	nsv541462	chr12:33528203-34491300	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
9	nsv1042712	chr12:33528204-34427733	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
10	nsv541463	chr12:33528204-34427733	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
11	nsv1047392	chr12:33528403-34427593	Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
12	nsv541464	chr12:33528403-34427593	Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
13	nsv1051183	chr12:33528403-34491152	Active TSS Bivalent/Poised TSS ZNF genes & repeats Enhancers Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
14	nsv541465	chr12:33528403-34491152	Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
15	nsv469350	chr12:33752330-34245756	Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
16	nsv558295	chr12:33752330-34245756	Active TSS Enhancers Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
17	nsv534000	chr12:33822185-34756209	Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
18	esv2830231	chr12:33826241-34801271	ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
19	nsv1040812	chr12:33863411-34854486	Bivalent Enhancer Active TSS Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
20	nsv1051316	chr12:33956561-34428933	Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Enhancers Weak transcription Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
21	nsv1051986	chr12:33962656-34457196	Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
22	nsv917816	chr12:33967852-34854486	ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
23	nsv1044382	chr12:33968178-34854486	Flanking Active TSS ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
24	nsv558297	chr12:34020094-34757810	Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription ZNF genes & repeats Strong transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
25	nsv533940	chr12:34023331-34756209	Enhancers ZNF genes & repeats Bivalent/Poised TSS Strong transcription Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
26	nsv1045677	chr12:34024348-34854486	Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
27	nsv1043754	chr12:34030026-34435009	Flanking Active TSS Bivalent/Poised TSS Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
28	nsv1037287	chr12:34030936-34491152	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Bivalent/Poised TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
29	nsv541471	chr12:34030936-34491152	ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Enhancers Strong transcription Weak transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
30	nsv915754	chr12:34052409-34756196	ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
31	nsv430503	chr12:34059018-34760333	Active TSS ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
32	nsv558298	chr12:34081127-34245756	Active TSS Flanking Active TSS Enhancers Weak transcription Strong transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
33	nsv558299	chr12:34081127-34252870	Enhancers Flanking Active TSS Strong transcription Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
34	nsv918189	chr12:34089213-34854486	Flanking Active TSS ZNF genes & repeats Enhancers Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
35	nsv1038502	chr12:34110609-34787964	Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Enhancers Flanking Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
36	nsv520568	chr12:34111494-34436391	Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
37	nsv527701	chr12:34111494-34819926	Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
38	nsv1045139	chr12:34125978-34854486	Active TSS Weak transcription ZNF genes & repeats Enhancers Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
39	nsv1036399	chr12:34160024-34854486	ZNF genes & repeats Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
40	nsv983459	chr12:34173918-34178625	Enhancers Flanking Active TSS Active TSS Strong transcription Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:117 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:34174200-34176000	Active TSS	Psoas Muscle	Psoas
2	chr12:34174400-34175800	Active TSS	Stomach Smooth Muscle	stomach
3	chr12:34174400-34175800	Active TSS	NH-A	brain
4	chr12:34174400-34176000	Active TSS	Brain Angular Gyrus	brain
5	chr12:34174400-34176000	Active TSS	Right Atrium	heart
6	chr12:34174400-34176200	Active TSS	NHDF-Ad	bronchial
7	chr12:34174400-34176400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr12:34174600-34175200	Flanking Active TSS	Dnd41	blood
9	chr12:34174600-34175200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
10	chr12:34174600-34175400	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr12:34174600-34175400	Active TSS	HepG2	liver
12	chr12:34174600-34175800	Active TSS	Primary T helper naive cells from peripheral blood	blood
13	chr12:34174600-34175800	Active TSS	Fetal Adrenal Gland	Adrenal Gland
14	chr12:34174600-34175800	Active TSS	Fetal Muscle Leg	muscle
15	chr12:34174600-34175800	Active TSS	Rectal Smooth Muscle	rectum
16	chr12:34174600-34175800	Active TSS	HUVEC	blood vessel
17	chr12:34174600-34175800	Active TSS	NHEK	skin
18	chr12:34174600-34175800	Active TSS	Osteobl	bone
19	chr12:34174600-34176000	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr12:34174600-34176000	Active TSS	Brain Anterior Caudate	brain
21	chr12:34174600-34176000	Active TSS	Brain Hippocampus Middle	brain
22	chr12:34174600-34176000	Active TSS	Brain Inferior Temporal Lobe	brain
23	chr12:34174600-34176000	Active TSS	Duodenum Smooth Muscle	Duodenum
24	chr12:34174600-34176000	Active TSS	Fetal Brain Male	brain
25	chr12:34174600-34176000	Active TSS	Fetal Brain Female	brain
26	chr12:34174600-34176000	Active TSS	Fetal Lung	lung
27	chr12:34174600-34176000	Active TSS	Fetal Stomach	stomach
28	chr12:34174600-34176000	Active TSS	Skeletal Muscle Male	skeletal muscle
29	chr12:34174600-34176000	Active TSS	Skeletal Muscle Female	skeletal muscle
30	chr12:34174600-34176200	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
31	chr12:34174600-34176200	Active TSS	Breast Myoepithelial Primary Cells	Breast
32	chr12:34174600-34176200	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr12:34174600-34176200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr12:34174600-34176200	Active TSS	Fetal Kidney	kidney
35	chr12:34174600-34176200	Active TSS	Pancreatic Islets	Pancreatic Islet
36	chr12:34174600-34176200	Active TSS	Fetal Muscle Trunk	muscle
37	chr12:34174600-34176200	Active TSS	GM12878-XiMat	blood
38	chr12:34174600-34176400	Active TSS	ES-I3 Cell Line	embryonic stem cell
39	chr12:34174600-34176400	Active TSS	Brain Germinal Matrix	brain
40	chr12:34174600-34176400	Active TSS	Rectal Mucosa Donor 29	rectum
41	chr12:34174600-34176400	Active TSS	NHLF	lung
42	chr12:34174600-34176600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr12:34174600-34176600	Active TSS	HUES48 Cell Line	embryonic stem cell
44	chr12:34174600-34176600	Active TSS	HUES6 Cell Line	embryonic stem cell
45	chr12:34174600-34176600	Active TSS	HUES64 Cell Line	embryonic stem cell
46	chr12:34174600-34176600	Active TSS	iPS-18 Cell Line	embryonic stem cell
47	chr12:34174600-34176600	Active TSS	iPS-20b Cell Line	embryonic stem cell
48	chr12:34174600-34176600	Active TSS	Muscle Satellite Cultured Cells	--
49	chr12:34174600-34176600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr12:34174600-34176600	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin

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