Variant report

Variant	rs10774481
Chromosome Location	chr12:1100637-1100638
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	POLR2A	chr12:1098467-1101358	MCF10A-Er-Src	breast:	n/a	n/a
2	CREB1	chr12:1099558-1100748	H1-hESC	embryonic stem cell:	n/a	n/a
3	POLR2A	chr12:1099401-1100668	HL-60	blood:	n/a	n/a
4	POLR2A	chr12:1099520-1100681	A549	lung:	n/a	n/a
5	POLR2A	chr12:1099603-1100667	HepG2	liver:	n/a	n/a
6	HEY1	chr12:1099542-1100719	HepG2	liver:	n/a	chr12:1099901-1099916 chr12:1099952-1099967
7	POLR2A	chr12:1099607-1100649	GM19193	blood:	n/a	n/a
8	MXI1	chr12:1098625-1101473	IMR90	lung:	n/a	n/a
9	MAX	chr12:1099452-1100797	MCF-7	breast:	n/a	n/a
10	POLR2A	chr12:1099082-1100758	K562	blood:	n/a	n/a
11	CCNT2	chr12:1099598-1100750	K562	blood:	n/a	chr12:1099952-1099961 chr12:1100669-1100678 chr12:1100693-1100702
12	POLR2A	chr12:1099490-1100644	K562	blood:	n/a	n/a
13	REST	chr12:1099411-1100663	HL-60	blood:	n/a	chr12:1099819-1099839 chr12:1100546-1100564 chr12:1100551-1100565
14	POLR2A	chr12:1099534-1100797	NB4	blood:	n/a	n/a
15	POLR2A	chr12:1099470-1100684	HCT-116	colon:	n/a	n/a
16	ZBTB7A	chr12:1099455-1101225	ECC-1	luminal epithelium:	n/a	chr12:1100728-1100739
17	SIN3A	chr12:1100594-1100778	GM12878	blood:	n/a	chr12:1100729-1100740 chr12:1100643-1100651
18	POLR2A	chr12:1099713-1100640	GM15510	blood:	n/a	n/a
19	CTCF	chr12:1100500-1100650	GM12871	blood:	n/a	n/a
20	TAF1	chr12:1099440-1100976	ECC-1	luminal epithelium:	n/a	n/a
21	NR3C1	chr12:1099520-1100907	A549	lung:	n/a	chr12:1099860-1099876 chr12:1099861-1099875 chr12:1099860-1099876
22	TBP	chr12:1099622-1100662	HepG2	liver:	n/a	n/a
23	CREB1	chr12:1099720-1100828	HepG2	liver:	n/a	n/a
24	TEAD4	chr12:1099487-1100825	ECC-1	luminal epithelium:	n/a	n/a
25	FOXP2	chr12:1099551-1100706	PFSK-1	brain:	n/a	n/a
26	TCF12	chr12:1099277-1100852	A549	lung:	n/a	n/a
27	POLR2A	chr12:1099695-1100655	GM18526	blood:	n/a	n/a
28	YY1	chr12:1099477-1100724	ECC-1	luminal epithelium:	n/a	chr12:1099768-1099782 chr12:1100693-1100704
29	POLR2A	chr12:1099575-1100687	GM19099	blood:	n/a	n/a
30	POLR2A	chr12:1100367-1100659	HepG2	liver:	n/a	n/a
31	MAX	chr12:1099299-1101097	ECC-1	luminal epithelium:	n/a	n/a
32	HMGN3	chr12:1099612-1100784	K562	blood:	n/a	n/a
33	MXI1	chr12:1099013-1100737	HepG2	liver:	n/a	n/a
34	TAF1	chr12:1099554-1100716	HepG2	liver:	n/a	n/a
35	CEBPD	chr12:1099766-1100782	HepG2	liver:	n/a	n/a
36	HCFC1	chr12:1098652-1101574	Hela-S3	cervix:	n/a	n/a
37	EP300	chr12:1099417-1100949	SK-N-SH	brain:	n/a	chr12:1100626-1100642 chr12:1100727-1100743 chr12:1099633-1099643
38	POLR2A	chr12:1099408-1101350	H1-hESC	embryonic stem cell:	n/a	n/a
39	SP1	chr12:1099028-1100958	A549	lung:	n/a	chr12:1099952-1099962 chr12:1100632-1100644 chr12:1100702-1100714 chr12:1099952-1099961 chr12:1100667-1100679 chr12:1099951-1099963 chr12:1100637-1100649 chr12:1100634-1100648 chr12:1100667-1100679 chr12:1099948-1099962 chr12:1100815-1100825 chr12:1100702-1100714 chr12:1100668-1100682 chr12:1100693-1100702 chr12:1099951-1099963 chr12:1099953-1099962 chr12:1100805-1100819 chr12:1099951-1099962 chr12:1100634-1100643 chr12:1100639-1100648 chr12:1100699-1100708 chr12:1100704-1100713 chr12:1099952-1099962 chr12:1100633-1100642 chr12:1100632-1100644 chr12:1100637-1100649 chr12:1100669-1100678
40	MAZ	chr12:1099671-1100718	HepG2	liver:	n/a	n/a
41	POLR2A	chr12:1099470-1100717	PFSK-1	brain:	n/a	n/a
42	GATA2	chr12:1100531-1101222	SH-SY5Y	brain:	n/a	chr12:1101007-1101028
43	YY1	chr12:1099538-1100817	ECC-1	luminal epithelium:	n/a	chr12:1100771-1100782 chr12:1099768-1099782 chr12:1100693-1100704
44	REST	chr12:1100022-1100864	H1-neurons	neurons:	n/a	chr12:1100546-1100564 chr12:1100551-1100565
45	POLR2A	chr12:1099509-1100775	HL-60	blood:	n/a	n/a
46	RFX5	chr12:1100476-1100692	HepG2	liver:	n/a	n/a
47	MYC	chr12:1099063-1100702	NB4	blood:	n/a	n/a
48	POLR2A	chr12:1098938-1101511	Hela-S3	cervix:	n/a	n/a
49	RCOR1	chr12:1099548-1101149	Hela-S3	cervix:	n/a	n/a
50	SIN3AK20	chr12:1100416-1100806	SK-N-SH	brain:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:1100598-1100648	GM12892	blood:	n/a
2	chr12:1100598-1100648	NT2-D1	testis:	n/a
3	chr12:1100598-1100648	NB4	blood:	n/a
4	chr12:1100598-1100648	HepG2	liver:	n/a
5	chr12:1100598-1100648	PFSK-1	brain:	n/a
6	chr12:1100598-1100648	RPTEC	kidney:	n/a
7	chr12:1100598-1100648	MCF10A-Er-Src	breast:	n/a
8	chr12:1100598-1100648	AG10803	skin:	n/a
9	chr12:1100598-1100648	PANC-1	pancreas:	n/a
10	chr12:1100598-1100648	AG09309	skin:	n/a
11	chr12:1100598-1100648	HEK293	kidney:	embryo
12	chr12:1100598-1100648	Caco-2	colon:	n/a
13	chr12:1100598-1100648	CMK	blood:	n/a
14	chr12:1100598-1100648	LNCaP	prostate:	n/a
15	chr12:1100598-1100648	PrEC	prostate:	n/a
16	chr12:1100598-1100648	AG04450	lung:	fetal
17	chr12:1100598-1100648	ProgFib	skin:	n/a
18	chr12:1100598-1100648	Hepatocyte	liver:	n/a
19	chr12:1100598-1100648	A549	lung:	n/a
20	chr12:1100598-1100648	HEEpiC	esophagus:	n/a
21	chr12:1100598-1100648	HUVEC	blood vessel:	n/a
22	chr12:1100598-1100648	AoSMC	blood vessel:	n/a
23	chr12:1100598-1100648	Jurkat	blood:	n/a
24	chr12:1100598-1100648	HNPCEpiC	eye:	n/a
25	chr12:1100598-1100648	BE2_C	brain:	n/a
26	chr12:1100598-1100648	SK-N-MC	brain:	n/a
27	chr12:1100598-1100648	HCF	heart:	n/a
28	chr12:1100598-1100648	AG09319	gingival:	n/a
29	chr12:1100598-1100648	SK-N-SH	brain:	n/a
30	chr12:1100598-1100648	HRPEpiC	eye:	n/a
31	chr12:1100598-1100648	HMEC	breast:	n/a
32	chr12:1100598-1100648	HIPEpiC	eye:	n/a
33	chr12:1100598-1100648	GM19239	blood:	n/a
34	chr12:1100598-1100648	HCM	heart:	n/a
35	chr12:1100598-1100648	HRCEpiC	kidney:	n/a
36	chr12:1100598-1100648	NHBE	bronchial:	n/a
37	chr12:1100598-1100648	NH-A	brain:	n/a
38	chr12:1100598-1100648	K562	blood:	n/a
39	chr12:1100598-1100648	IMR90	lung:	fetal
40	chr12:1100598-1100648	HCT-116	colon:	n/a
41	chr12:1100598-1100648	HAEpiC	amniotic membrane:	n/a
42	chr12:1100598-1100648	U87	brain:	n/a
43	chr12:1100598-1100648	HRE	kidney:	n/a
44	chr12:1100598-1100648	HCPEpiC	choroid plexus:	n/a
45	chr12:1100598-1100648	SAEC	small airway:	n/a
46	chr12:1100598-1100648	AG04449	skin:	fetal
47	chr12:1100598-1100648	HPAEpiC	pulmonary alveolar:	n/a
48	chr12:1100598-1100648	NHDF-neo	bronchial:	n/a
49	chr12:1100598-1100648	GM06990	blood:	n/a
50	chr12:1100598-1100648	BJ	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:1057369..1058961-chr12:1099742..1102215,2	K562	blood:
2	chr12:1099319..1102192-chr19:46282612..46285259,2	MCF-7	breast:
3	chr1:46152739..46153727-chr12:1100153..1101024,2	NB4	blood:
4	chr12:1100504..1101231-chr17:26368491..26369260,2	Hela-S3	cervix:
5	chr12:1100048..1100689-chr2:47168066..47168566,2	HCT-116	colon:
6	chr12:1100265..1100782-chr2:47168046..47168566,2	MCF-7	breast:
7	chr12:1100058..1100987-chr16:89119009..89119720,2	Hela-S3	cervix:
8	chr12:1099879..1100771-chr5:137673557..137674488,2	Hela-S3	cervix:
9	chr12:1056985..1060702-chr12:1098122..1101434,9	MCF-7	breast:
10	chr1:149859365..149860018-chr12:1100150..1100668,2	Hela-S3	cervix:
11	chr12:1100037..1100656-chr12:51442773..51443406,2	Hela-S3	cervix:
12	chr12:1097166..1102781-chr12:1103327..1109862,10	MCF-7	breast:
13	chr10:92617261..92617781-chr12:1100112..1100745,2	HCT-116	colon:

Variant related genes	Relation type
ENSG00000250132	TF binding region
RAD52	TF binding region
ERC1	TF binding region
ERC1	CpG island
ENSG00000250132	CpG island
RAD52	CpG island
ENSG00000184270	Chromatin interaction
ENSG00000104936	Chromatin interaction
ENSG00000050426	Chromatin interaction
ENSG00000002016	Chromatin interaction
ENSG00000082805	Chromatin interaction
ENSG00000178096	Chromatin interaction
ENSG00000087095	Chromatin interaction
ENSG00000256982	Chromatin interaction
ENSG00000148680	Chromatin interaction
ENSG00000159592	Chromatin interaction
ENSG00000158402	Chromatin interaction
ENSG00000159596	Chromatin interaction
ENSG00000068724	Chromatin interaction
ENSG00000120709	Chromatin interaction

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10849612	0.92[AMR][1000 genomes];0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs10849620	0.85[AMR][1000 genomes]
rs11064634	0.80[ASN][1000 genomes]
rs12370704	0.92[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12811563	0.84[AMR][1000 genomes]
rs2079299	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2097859	0.83[AMR][1000 genomes]
rs4765965	0.80[AMR][1000 genomes]
rs4765969	0.81[AMR][1000 genomes]
rs6489255	0.80[AMR][1000 genomes]
rs7311276	0.81[AMR][1000 genomes]
rs7954121	0.80[AMR][1000 genomes]
rs7956944	0.83[AMR][1000 genomes]
rs7974198	0.82[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:29 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1049944	chr12:282465-1232077	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer 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 miRNA target site	80 gene(s)	inside rSNPs	diseases
2	nsv541306	chr12:282465-1232077	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
3	nsv949469	chr12:380411-1122450	Enhancers Strong transcription Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
4	nsv556892	chr12:673515-1210884	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
5	nsv898576	chr12:813411-1553450	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
6	nsv948760	chr12:863833-1542875	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
7	nsv1052589	chr12:910460-1421493	ZNF genes & repeats Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
8	nsv1045278	chr12:920251-1697030	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
9	nsv529398	chr12:941915-1741311	Weak transcription Strong transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
10	nsv468960	chr12:975276-1455106	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
11	nsv556941	chr12:975276-1455106	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers 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 target site	33 gene(s)	inside rSNPs	diseases
12	nsv1044329	chr12:985144-1403020	Genic enhancers Weak transcription Enhancers Active TSS Bivalent Enhancer Strong transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
13	nsv541340	chr12:985144-1403020	Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
14	nsv470256	chr12:998365-1438761	Enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
15	nsv492321	chr12:1011692-1388512	Weak transcription Active TSS Enhancers Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
16	nsv898579	chr12:1013176-1510505	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
17	nsv898580	chr12:1024688-1569097	Weak transcription Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
18	nsv1036488	chr12:1041097-1445923	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
19	nsv1037825	chr12:1045734-1432940	Bivalent/Poised TSS Weak transcription Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
20	nsv541342	chr12:1045734-1432940	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 Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
21	nsv868854	chr12:1045935-1354083	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
22	nsv468962	chr12:1047531-1119958	Flanking Active TSS Weak transcription Enhancers Active TSS Genic enhancers ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
23	nsv556942	chr12:1047531-1119958	Flanking Active TSS Weak transcription Active TSS Strong transcription Enhancers Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
24	esv2762958	chr12:1049279-1554962	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
25	nsv1052559	chr12:1077964-1588543	Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
26	nsv898581	chr12:1084783-1527359	Flanking Active TSS Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
27	nsv1041799	chr12:1091294-1304839	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
28	nsv541343	chr12:1091294-1304839	Flanking Active TSS Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
29	esv3357464	chr12:1099316-1101864	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	22 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	chr12:1098600-1101200	Active TSS	Psoas Muscle	Psoas
2	chr12:1098600-1101600	Active TSS	Aorta	Aorta
3	chr12:1098600-1101800	Active TSS	Fetal Brain Male	brain
4	chr12:1098800-1101200	Active TSS	Ovary	ovary
5	chr12:1098800-1101400	Active TSS	Breast Myoepithelial Primary Cells	Breast
6	chr12:1098800-1101600	Active TSS	Left Ventricle	heart
7	chr12:1098800-1101600	Active TSS	Right Ventricle	heart
8	chr12:1098800-1101800	Active TSS	Duodenum Smooth Muscle	Duodenum
9	chr12:1099000-1101000	Active TSS	Fetal Brain Female	brain
10	chr12:1099000-1101200	Active TSS	Colonic Mucosa	Colon
11	chr12:1099000-1101200	Active TSS	Esophagus	oesophagus
12	chr12:1099000-1101200	Active TSS	Lung	lung
13	chr12:1099000-1101600	Active TSS	H9 Cell Line	embryonic stem cell
14	chr12:1099000-1101600	Active TSS	Fetal Muscle Trunk	muscle
15	chr12:1099000-1101800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr12:1099000-1101800	Active TSS	Pancreatic Islets	Pancreatic Islet
17	chr12:1099200-1101000	Active TSS	Skeletal Muscle Male	skeletal muscle
18	chr12:1099200-1101000	Active TSS	Stomach Mucosa	stomach
19	chr12:1099200-1101000	Active TSS	K562	blood
20	chr12:1099200-1101200	Active TSS	Brain Cingulate Gyrus	brain
21	chr12:1099200-1101200	Active TSS	Brain Hippocampus Middle	brain
22	chr12:1099200-1101200	Active TSS	Fetal Intestine Small	intestine
23	chr12:1099200-1101200	Active TSS	Fetal Stomach	stomach
24	chr12:1099200-1101200	Active TSS	Sigmoid Colon	Sigmoid Colon
25	chr12:1099200-1101200	Active TSS	Stomach Smooth Muscle	stomach
26	chr12:1099200-1101400	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr12:1099200-1101400	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr12:1099200-1101400	Active TSS	Colon Smooth Muscle	Colon
29	chr12:1099200-1101400	Active TSS	Fetal Intestine Large	intestine
30	chr12:1099200-1101600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr12:1099200-1101600	Active TSS	Thymus	Thymus
32	chr12:1099200-1101800	Active TSS	ES-I3 Cell Line	embryonic stem cell
33	chr12:1099200-1101800	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr12:1099200-1101800	Active TSS	Fetal Kidney	kidney
35	chr12:1099200-1102000	Active TSS	Brain Angular Gyrus	brain
36	chr12:1099200-1102000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
37	chr12:1099400-1100800	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
38	chr12:1099400-1101000	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr12:1099400-1101000	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr12:1099400-1101000	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr12:1099400-1101000	Active TSS	Liver	Liver
42	chr12:1099400-1101000	Active TSS	Duodenum Mucosa	Duodenum
43	chr12:1099400-1101000	Active TSS	Fetal Lung	lung
44	chr12:1099400-1101000	Active TSS	Placenta Amnion	Placenta Amnion
45	chr12:1099400-1101000	Active TSS	Rectal Mucosa Donor 29	rectum
46	chr12:1099400-1101000	Active TSS	Rectal Mucosa Donor 31	rectum
47	chr12:1099400-1101200	Active TSS	HUES64 Cell Line	embryonic stem cell
48	chr12:1099400-1101200	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
49	chr12:1099400-1101200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr12:1099400-1101200	Active TSS	Primary T helper memory cells from peripheral blood 2	blood

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