Variant report

Variant	rs11168981
Chromosome Location	chr12:49740532-49740533
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	chr12:49740402-49742031	MCF-7	breast:	n/a	n/a
2	MAX	chr12:49740385-49742027	ECC-1	luminal epithelium:	n/a	n/a
3	TCF12	chr12:49740213-49742052	ECC-1	luminal epithelium:	n/a	chr12:49741032-49741042
4	MAX	chr12:49740435-49742080	A549	lung:	n/a	n/a
5	ZBTB7A	chr12:49738646-49742163	ECC-1	luminal epithelium:	n/a	chr12:49739274-49739281 chr12:49741924-49741935 chr12:49741555-49741564
6	ELF1	chr12:49740480-49740867	K562	blood:	n/a	chr12:49740521-49740530 chr12:49740514-49740526 chr12:49740513-49740525 chr12:49740517-49740529 chr12:49740484-49740496
7	POLR2A	chr12:49740405-49740885	K562	blood:	n/a	n/a
8	TCF12	chr12:49740418-49742001	ECC-1	luminal epithelium:	n/a	chr12:49741032-49741042
9	FOXA1	chr12:49740399-49740588	T-47D	breast:	n/a	n/a
10	ZBTB7A	chr12:49740332-49740593	HepG2	liver:	n/a	n/a
11	POLR2A	chr12:49740309-49740868	K562	blood:	n/a	n/a
12	UBTF	chr12:49740420-49741077	K562	blood:	n/a	n/a
13	E2F6	chr12:49740400-49741117	K562	blood:	n/a	chr12:49740463-49740473 chr12:49740739-49740750 chr12:49740613-49740622 chr12:49740466-49740476 chr12:49740519-49740529
14	EGR1	chr12:49739483-49741923	MCF-7	breast:	n/a	chr12:49740466-49740479 chr12:49740522-49740536 chr12:49740007-49740020 chr12:49740612-49740622 chr12:49740520-49740542 chr12:49739746-49739759 chr12:49740608-49740621 chr12:49739998-49740008 chr12:49740466-49740479 chr12:49739743-49739757 chr12:49740526-49740536 chr12:49739747-49739757 chr12:49740608-49740621 chr12:49740525-49740538 chr12:49740524-49740538 chr12:49739747-49739757 chr12:49741709-49741719 chr12:49739746-49739759 chr12:49740799-49740812 chr12:49740007-49740017 chr12:49740608-49740618 chr12:49740526-49740536 chr12:49740526-49740537 chr12:49740608-49740621 chr12:49739976-49739990 chr12:49739745-49739759 chr12:49740461-49740483 chr12:49740006-49740021 chr12:49740609-49740618 chr12:49739746-49739759 chr12:49740607-49740622 chr12:49739747-49739756 chr12:49740607-49740621 chr12:49740525-49740538 chr12:49740613-49740623 chr12:49740467-49740476 chr12:49740466-49740479 chr12:49740466-49740476 chr12:49740608-49740621 chr12:49740004-49740018 chr12:49740526-49740537 chr12:49739747-49739758 chr12:49740525-49740538 chr12:49740526-49740535
15	MAX	chr12:49740476-49740833	K562	blood:	n/a	n/a
16	EGR1	chr12:49740153-49740973	HCT-116	colon:	n/a	chr12:49740466-49740479 chr12:49740522-49740536 chr12:49740612-49740622 chr12:49740520-49740542 chr12:49740608-49740621 chr12:49740466-49740479 chr12:49740526-49740536 chr12:49740608-49740621 chr12:49740525-49740538 chr12:49740524-49740538 chr12:49740799-49740812 chr12:49740608-49740618 chr12:49740526-49740536 chr12:49740526-49740537 chr12:49740608-49740621 chr12:49740461-49740483 chr12:49740609-49740618 chr12:49740607-49740622 chr12:49740607-49740621 chr12:49740525-49740538 chr12:49740613-49740623 chr12:49740467-49740476 chr12:49740466-49740479 chr12:49740466-49740476 chr12:49740608-49740621 chr12:49740526-49740537 chr12:49740525-49740538 chr12:49740526-49740535
17	FOXA1	chr12:49740429-49740626	ECC-1	luminal epithelium:	n/a	n/a
18	HDAC2	chr12:49740223-49742034	MCF-7	breast:	n/a	n/a
19	SMC3	chr12:49740372-49742164	SK-N-SH	brain:	n/a	chr12:49741556-49741570 chr12:49741556-49741566 chr12:49741019-49741027
20	MAX	chr12:49740347-49741727	K562	blood:	n/a	n/a
21	EGR1	chr12:49739727-49740749	H1-hESC	embryonic stem cell:	n/a	chr12:49740466-49740479 chr12:49740522-49740536 chr12:49740007-49740020 chr12:49740612-49740622 chr12:49740520-49740542 chr12:49739746-49739759 chr12:49740608-49740621 chr12:49739998-49740008 chr12:49740466-49740479 chr12:49739743-49739757 chr12:49740526-49740536 chr12:49739747-49739757 chr12:49740608-49740621 chr12:49740525-49740538 chr12:49740524-49740538 chr12:49739747-49739757 chr12:49739746-49739759 chr12:49740007-49740017 chr12:49740608-49740618 chr12:49740526-49740536 chr12:49740526-49740537 chr12:49740608-49740621 chr12:49739976-49739990 chr12:49739745-49739759 chr12:49740461-49740483 chr12:49740006-49740021 chr12:49740609-49740618 chr12:49739746-49739759 chr12:49740607-49740622 chr12:49739747-49739756 chr12:49740607-49740621 chr12:49740525-49740538 chr12:49740613-49740623 chr12:49740467-49740476 chr12:49740466-49740479 chr12:49740466-49740476 chr12:49740608-49740621 chr12:49740004-49740018 chr12:49740526-49740537 chr12:49739747-49739758 chr12:49740525-49740538 chr12:49740526-49740535
22	EGR1	chr12:49740374-49740668	GM12878	blood:	n/a	chr12:49740466-49740479 chr12:49740522-49740536 chr12:49740612-49740622 chr12:49740520-49740542 chr12:49740608-49740621 chr12:49740466-49740479 chr12:49740526-49740536 chr12:49740608-49740621 chr12:49740525-49740538 chr12:49740524-49740538 chr12:49740608-49740618 chr12:49740526-49740536 chr12:49740526-49740537 chr12:49740608-49740621 chr12:49740461-49740483 chr12:49740609-49740618 chr12:49740607-49740622 chr12:49740607-49740621 chr12:49740525-49740538 chr12:49740613-49740623 chr12:49740467-49740476 chr12:49740466-49740479 chr12:49740466-49740476 chr12:49740608-49740621 chr12:49740526-49740537 chr12:49740525-49740538 chr12:49740526-49740535
23	YY1	chr12:49740401-49740625	K562	blood:	n/a	chr12:49740610-49740619 chr12:49740513-49740527 chr12:49740515-49740529 chr12:49740510-49740524 chr12:49740468-49740477 chr12:49740518-49740527 chr12:49740516-49740530 chr12:49740521-49740530 chr12:49740463-49740477 chr12:49740613-49740622 chr12:49740610-49740621 chr12:49740462-49740476 chr12:49740468-49740479
24	MAZ	chr12:49740407-49741813	K562	blood:	n/a	n/a
25	FOXA1	chr12:49740367-49740668	HepG2	liver:	n/a	n/a
26	CTCF	chr12:49740404-49742833	A549	lung:	n/a	chr12:49741554-49741572 chr12:49741549-49741570 chr12:49740510-49740523 chr12:49741555-49741571 chr12:49741556-49741569 chr12:49741556-49741569
27	HA-E2F1	chr12:49740350-49740954	MCF-7	breast:	n/a	chr12:49740463-49740473 chr12:49740613-49740622 chr12:49740466-49740476 chr12:49740519-49740529
28	CTBP2	chr12:49739324-49741267	H1-hESC	embryonic stem cell:	n/a	n/a
29	HMGN3	chr12:49740376-49740671	K562	blood:	n/a	n/a
30	EGR1	chr12:49740235-49740938	HCT-116	colon:	n/a	chr12:49740466-49740479 chr12:49740522-49740536 chr12:49740612-49740622 chr12:49740520-49740542 chr12:49740608-49740621 chr12:49740466-49740479 chr12:49740526-49740536 chr12:49740608-49740621 chr12:49740525-49740538 chr12:49740524-49740538 chr12:49740799-49740812 chr12:49740608-49740618 chr12:49740526-49740536 chr12:49740526-49740537 chr12:49740608-49740621 chr12:49740461-49740483 chr12:49740609-49740618 chr12:49740607-49740622 chr12:49740607-49740621 chr12:49740525-49740538 chr12:49740613-49740623 chr12:49740467-49740476 chr12:49740466-49740479 chr12:49740466-49740476 chr12:49740608-49740621 chr12:49740526-49740537 chr12:49740525-49740538 chr12:49740526-49740535
31	NFIC	chr12:49740284-49741942	ECC-1	luminal epithelium:	n/a	n/a
32	POLR2A	chr12:49739596-49741075	H1-neurons	neurons:	n/a	n/a
33	YY1	chr12:49740365-49740710	K562	blood:	n/a	chr12:49740610-49740619 chr12:49740513-49740527 chr12:49740515-49740529 chr12:49740510-49740524 chr12:49740468-49740477 chr12:49740518-49740527 chr12:49740516-49740530 chr12:49740521-49740530 chr12:49740463-49740477 chr12:49740613-49740622 chr12:49740610-49740621 chr12:49740462-49740476 chr12:49740468-49740479
34	EGR1	chr12:49740277-49740813	K562	blood:	n/a	chr12:49740466-49740479 chr12:49740522-49740536 chr12:49740612-49740622 chr12:49740520-49740542 chr12:49740608-49740621 chr12:49740466-49740479 chr12:49740526-49740536 chr12:49740608-49740621 chr12:49740525-49740538 chr12:49740524-49740538 chr12:49740799-49740812 chr12:49740608-49740618 chr12:49740526-49740536 chr12:49740526-49740537 chr12:49740608-49740621 chr12:49740461-49740483 chr12:49740609-49740618 chr12:49740607-49740622 chr12:49740607-49740621 chr12:49740525-49740538 chr12:49740613-49740623 chr12:49740467-49740476 chr12:49740466-49740479 chr12:49740466-49740476 chr12:49740608-49740621 chr12:49740526-49740537 chr12:49740525-49740538 chr12:49740526-49740535
35	ELF1	chr12:49740233-49740827	K562	blood:	n/a	chr12:49740521-49740530 chr12:49740514-49740526 chr12:49740513-49740525 chr12:49740517-49740529 chr12:49740464-49740476 chr12:49740484-49740496
36	ZBTB7A	chr12:49738673-49741889	ECC-1	luminal epithelium:	n/a	chr12:49739274-49739281 chr12:49741555-49741564
37	SUZ12	chr12:49738478-49741665	NT2-D1	testis:	n/a	n/a
38	CCNT2	chr12:49740392-49740569	K562	blood:	n/a	n/a
39	MAX	chr12:49740356-49742248	A549	lung:	n/a	n/a
40	TAF1	chr12:49740338-49740767	K562	blood:	n/a	n/a
41	FOXA2	chr12:49740390-49740684	HepG2	liver:	n/a	n/a
42	MAX	chr12:49740433-49741975	HepG2	liver:	n/a	n/a
43	ELF1	chr12:49740235-49741766	GM12878	blood:	n/a	chr12:49740521-49740530 chr12:49740514-49740526 chr12:49740513-49740525 chr12:49740517-49740529 chr12:49740464-49740476 chr12:49740484-49740496 chr12:49741594-49741606 chr12:49741549-49741558
44	E2F6	chr12:49740428-49741938	A549	lung:	n/a	chr12:49740463-49740473 chr12:49741671-49741683 chr12:49740739-49740750 chr12:49740613-49740622 chr12:49740466-49740476 chr12:49740519-49740529
45	ATF3	chr12:49740347-49740608	K562	blood:	n/a	n/a
46	EGR1	chr12:49740150-49741821	MCF-7	breast:	n/a	chr12:49740466-49740479 chr12:49740522-49740536 chr12:49740612-49740622 chr12:49740520-49740542 chr12:49740608-49740621 chr12:49740466-49740479 chr12:49740526-49740536 chr12:49740608-49740621 chr12:49740525-49740538 chr12:49740524-49740538 chr12:49741709-49741719 chr12:49740799-49740812 chr12:49740608-49740618 chr12:49740526-49740536 chr12:49740526-49740537 chr12:49740608-49740621 chr12:49740461-49740483 chr12:49740609-49740618 chr12:49740607-49740622 chr12:49740607-49740621 chr12:49740525-49740538 chr12:49740613-49740623 chr12:49740467-49740476 chr12:49740466-49740479 chr12:49740466-49740476 chr12:49740608-49740621 chr12:49740526-49740537 chr12:49740525-49740538 chr12:49740526-49740535
47	EGR1	chr12:49740214-49740846	K562	blood:	n/a	chr12:49740466-49740479 chr12:49740522-49740536 chr12:49740612-49740622 chr12:49740520-49740542 chr12:49740608-49740621 chr12:49740466-49740479 chr12:49740526-49740536 chr12:49740608-49740621 chr12:49740525-49740538 chr12:49740524-49740538 chr12:49740799-49740812 chr12:49740608-49740618 chr12:49740526-49740536 chr12:49740526-49740537 chr12:49740608-49740621 chr12:49740461-49740483 chr12:49740609-49740618 chr12:49740607-49740622 chr12:49740607-49740621 chr12:49740525-49740538 chr12:49740613-49740623 chr12:49740467-49740476 chr12:49740466-49740479 chr12:49740466-49740476 chr12:49740608-49740621 chr12:49740526-49740537 chr12:49740525-49740538 chr12:49740526-49740535
48	CTCF	chr12:49740516-49742057	SK-N-SH	brain:	n/a	chr12:49741554-49741572 chr12:49741549-49741570 chr12:49741555-49741571 chr12:49741556-49741569 chr12:49741556-49741569
49	EGR1	chr12:49740351-49740732	GM12878	blood:	n/a	chr12:49740466-49740479 chr12:49740522-49740536 chr12:49740612-49740622 chr12:49740520-49740542 chr12:49740608-49740621 chr12:49740466-49740479 chr12:49740526-49740536 chr12:49740608-49740621 chr12:49740525-49740538 chr12:49740524-49740538 chr12:49740608-49740618 chr12:49740526-49740536 chr12:49740526-49740537 chr12:49740608-49740621 chr12:49740461-49740483 chr12:49740609-49740618 chr12:49740607-49740622 chr12:49740607-49740621 chr12:49740525-49740538 chr12:49740613-49740623 chr12:49740467-49740476 chr12:49740466-49740479 chr12:49740466-49740476 chr12:49740608-49740621 chr12:49740526-49740537 chr12:49740525-49740538 chr12:49740526-49740535
50	TCF12	chr12:49740483-49742251	A549	lung:	n/a	chr12:49741032-49741042 chr12:49742192-49742199

No.	Distal block	Cell Line	Cell type
1	chr12:49739423..49741666-chr12:49907974..49910735,2	MCF-7	breast:
2	chr12:49656587..49660636-chr12:49733539..49743833,13	K562	blood:
3	chr12:49737598..49740843-chr12:49959274..49963250,5	K562	blood:
4	chr12:49739131..49745064-chr12:49758784..49762517,10	MCF-7	breast:
5	chr12:49657182..49662198-chr12:49738070..49742868,13	MCF-7	breast:
6	chr12:49740075..49745225-chr12:49756992..49761732,8	K562	blood:
7	chr12:49740266..49744152-chr12:49960185..49963713,4	MCF-7	breast:
8	chr12:49715312..49722303-chr12:49739075..49744198,13	MCF-7	breast:
9	chr12:49740264..49744957-chr12:49759411..49762039,7	MCF-7	breast:
10	chr12:49655321..49661148-chr12:49729487..49743115,26	K562	blood:
11	chr12:49738282..49740573-chr12:49961441..49963250,2	K562	blood:
12	chr12:49656742..49663815-chr12:49736558..49745017,19	MCF-7	breast:

Variant related genes	Relation type
DNAJC22	TF binding region
ENSG00000258101	Chromatin interaction
ENSG00000110844	Chromatin interaction
ENSG00000167553	Chromatin interaction
ENSG00000258334	Chromatin interaction
ENSG00000123352	Chromatin interaction
ENSG00000135451	Chromatin interaction
ENSG00000187778	Chromatin interaction

Extended variants
information (count: 68 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:60)

rs_ID	r²[population]
rs10400435	0.82[CHB][hapmap]
rs10506284	1.00[JPT][hapmap]
rs10506285	1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs11168975	0.82[CHB][hapmap]
rs11169005	1.00[LWK][hapmap]
rs11169016	1.00[JPT][hapmap];0.87[MEX][hapmap]
rs11169058	1.00[JPT][hapmap]
rs11169059	1.00[JPT][hapmap]
rs11169063	0.85[LWK][hapmap]
rs11831313	0.88[ASN][1000 genomes]
rs11834161	1.00[JPT][hapmap]
rs11835071	0.82[ASN][1000 genomes]
rs11835303	0.82[CHB][hapmap]
rs12296440	1.00[JPT][hapmap]
rs12299777	0.94[ASN][1000 genomes]
rs12301632	1.00[JPT][hapmap];0.81[MEX][hapmap]
rs12305716	1.00[JPT][hapmap]
rs12306118	1.00[JPT][hapmap];0.81[MEX][hapmap]
rs12306866	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs12309053	1.00[JPT][hapmap]
rs12310129	1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs12315996	1.00[JPT][hapmap];0.81[MEX][hapmap]
rs12317856	0.88[ASN][1000 genomes]
rs12322561	1.00[JPT][hapmap]
rs12580931	0.82[CHB][hapmap]
rs12822293	0.82[CHB][hapmap]
rs17123696	1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs1874909	0.94[ASN][1000 genomes]
rs1874910	1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs1874911	0.94[ASN][1000 genomes]
rs2270741	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs2272478	1.00[JPT][hapmap];0.81[MEX][hapmap]
rs3088008	0.82[CHB][hapmap]
rs4243545	0.82[CHB][hapmap]
rs4898519	0.82[CHB][hapmap]
rs60331259	0.88[ASN][1000 genomes]
rs60494978	0.88[ASN][1000 genomes]
rs6580707	1.00[JPT][hapmap];0.81[MEX][hapmap]
rs6580709	1.00[JPT][hapmap];0.81[MEX][hapmap]
rs6580716	1.00[JPT][hapmap]
rs7133398	0.90[LWK][hapmap]
rs7139061	1.00[JPT][hapmap]
rs7294648	1.00[JPT][hapmap];0.81[MEX][hapmap]
rs7294973	1.00[JPT][hapmap]
rs7295162	1.00[JPT][hapmap]
rs7295556	0.83[LWK][hapmap]
rs7309997	1.00[JPT][hapmap]
rs7310682	0.94[CEU][hapmap];1.00[YRI][hapmap];0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7342365	1.00[JPT][hapmap]
rs74089059	1.00[ASN][1000 genomes]
rs74089062	0.94[ASN][1000 genomes]
rs7955245	0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7955541	1.00[JPT][hapmap];0.81[MEX][hapmap]
rs7962951	1.00[JPT][hapmap];0.81[MEX][hapmap]
rs7969099	1.00[JPT][hapmap];0.81[MEX][hapmap]
rs7974420	1.00[LWK][hapmap];0.81[MEX][hapmap];0.81[MKK][hapmap]
rs7975712	0.97[LWK][hapmap]
rs7976165	1.00[JPT][hapmap]
rs7980731	0.94[LWK][hapmap];0.81[MEX][hapmap]
rs9919740	1.00[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1051161	chr12:49314550-49828473	Flanking Bivalent TSS/Enh Weak transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Active TSS Strong transcription Enhancers Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	322 gene(s)	inside rSNPs	diseases
2	nsv541489	chr12:49314550-49828473	Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers Weak transcription Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	322 gene(s)	inside rSNPs	diseases
3	nsv1036452	chr12:49376285-49867760	Weak transcription Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	315 gene(s)	inside rSNPs	diseases
4	nsv428801	chr12:49536659-49744884	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Weak transcription Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	145 gene(s)	inside rSNPs	diseases
5	nsv1042122	chr12:49678529-49823168	Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Enhancers Active TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	54 gene(s)	inside rSNPs	diseases
6	nsv1039176	chr12:49678529-49832618	Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	55 gene(s)	inside rSNPs	diseases
7	nsv899068	chr12:49714103-49924637	Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
8	nsv832405	chr12:49720279-49910862	Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:121 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:49738400-49740800	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
2	chr12:49738600-49741200	Bivalent Enhancer	Fetal Brain Male	brain
3	chr12:49738800-49740800	Bivalent Enhancer	Fetal Heart	heart
4	chr12:49738800-49741000	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
5	chr12:49738800-49741400	Bivalent Enhancer	Fetal Thymus	thymus
6	chr12:49738800-49741800	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
7	chr12:49738800-49742000	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
8	chr12:49738800-49742000	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
9	chr12:49738800-49742000	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
10	chr12:49739000-49741200	Bivalent Enhancer	Small Intestine	intestine
11	chr12:49739000-49741400	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr12:49739000-49741800	Active TSS	Aorta	Aorta
13	chr12:49739000-49742000	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr12:49739000-49742000	Enhancers	Lung	lung
15	chr12:49739000-49742200	Active TSS	Pancreatic Islets	Pancreatic Islet
16	chr12:49739200-49742000	Flanking Bivalent TSS/Enh	Colonic Mucosa	Colon
17	chr12:49739200-49742200	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
18	chr12:49739400-49740600	Bivalent Enhancer	Esophagus	oesophagus
19	chr12:49739400-49741000	Bivalent/Poised TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr12:49739400-49741000	Flanking Bivalent TSS/Enh	NH-A	brain
21	chr12:49739400-49741200	Flanking Bivalent TSS/Enh	Cortex derived primary cultured neurospheres	brain
22	chr12:49739400-49741200	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
23	chr12:49739400-49741200	Flanking Active TSS	Ovary	ovary
24	chr12:49739400-49741200	Bivalent Enhancer	Sigmoid Colon	Sigmoid Colon
25	chr12:49739400-49741400	Flanking Bivalent TSS/Enh	Muscle Satellite Cultured Cells	--
26	chr12:49739400-49741400	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr12:49739400-49741400	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr12:49739400-49741400	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr12:49739400-49741600	Flanking Bivalent TSS/Enh	Primary T helper cells fromperipheralblood	blood
30	chr12:49739400-49741600	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr12:49739400-49741800	Flanking Bivalent TSS/Enh	Primary T helper naive cells fromperipheralblood	blood
32	chr12:49739400-49741800	Flanking Bivalent TSS/Enh	Primary T helper 17 cells PMA-I stimulated	--
33	chr12:49739400-49741800	Flanking Bivalent TSS/Enh	Primary T regulatory cells fromperipheralblood	blood
34	chr12:49739400-49741800	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr12:49739400-49741800	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr12:49739400-49741800	Flanking Bivalent TSS/Enh	Brain Cingulate Gyrus	brain
37	chr12:49739400-49742000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
38	chr12:49739400-49742000	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
39	chr12:49739400-49742000	Flanking Bivalent TSS/Enh	Duodenum Smooth Muscle	Duodenum
40	chr12:49739400-49742000	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
41	chr12:49739400-49742200	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr12:49739600-49740600	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood
43	chr12:49739600-49740600	Bivalent Enhancer	Placenta Amnion	Placenta Amnion
44	chr12:49739600-49741200	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr12:49739600-49741400	Enhancers	Gastric	stomach
46	chr12:49739600-49742400	Flanking Bivalent TSS/Enh	Brain Hippocampus Middle	brain
47	chr12:49739800-49740600	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
48	chr12:49739800-49740600	Bivalent/Poised TSS	iPS DF 6.9 Cell Line	embryonic stem cell
49	chr12:49739800-49740600	Active TSS	Breast Myoepithelial Primary Cells	Breast
50	chr12:49739800-49740600	Flanking Active TSS	Primary hematopoietic stem cells	blood

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