Variant report

Variant	rs11571377
Chromosome Location	chr12:1059429-1059430
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	YY1	chr12:1058132-1059550	H1-hESC	embryonic stem cell:	n/a	chr12:1058667-1058678
2	CTCF	chr12:1058977-1059439	K562	blood:	n/a	chr12:1059130-1059140 chr12:1059129-1059142 chr12:1059133-1059142 chr12:1059122-1059143 chr12:1059127-1059145
3	CTCF	chr12:1058959-1059478	GM19240	blood:	n/a	chr12:1059130-1059140 chr12:1059129-1059142 chr12:1059133-1059142 chr12:1059122-1059143 chr12:1059127-1059145
4	CTCF	chr12:1058896-1059474	SK-N-SH_RA	brain:	n/a	chr12:1059130-1059140 chr12:1059129-1059142 chr12:1059133-1059142 chr12:1059122-1059143 chr12:1059127-1059145
5	POLR2A	chr12:1057717-1059641	GM12892	blood:	n/a	n/a
6	MAX	chr12:1058097-1059555	H1-hESC	embryonic stem cell:	n/a	n/a
7	ELF1	chr12:1058232-1059636	GM12878	blood:	n/a	chr12:1058688-1058697 chr12:1058687-1058698
8	POLR2A	chr12:1057361-1059459	GM12891	blood:	n/a	n/a
9	ATF3	chr12:1058603-1059472	H1-hESC	embryonic stem cell:	n/a	n/a
10	EBF1	chr12:1058990-1059636	GM12878	blood:	n/a	chr12:1059446-1059457
11	POLR2A	chr12:1058160-1059613	H1-hESC	embryonic stem cell:	n/a	n/a
12	POLR2A	chr12:1059225-1059439	A549	lung:	n/a	n/a
13	CREB1	chr12:1058136-1059516	A549	lung:	n/a	n/a
14	EP300	chr12:1058555-1059554	GM12878	blood:	n/a	chr12:1059224-1059233
15	POLR2A	chr12:1058195-1059511	H1-hESC	embryonic stem cell:	n/a	n/a
16	POLR2A	chr12:1057952-1059583	GM12892	blood:	n/a	n/a
17	ZNF143	chr12:1058184-1059535	GM12878	blood:	n/a	chr12:1058380-1058399
18	POLR2A	chr12:1058079-1059452	GM12878	blood:	n/a	n/a
19	POLR2A	chr12:1057915-1059530	HL-60	blood:	n/a	n/a
20	CTCF	chr12:1059344-1059429	MCF-7	breast:	n/a	n/a
21	RCOR1	chr12:1058183-1059620	GM12878	blood:	n/a	n/a
22	CTCF	chr12:1058956-1059458	A549	lung:	n/a	chr12:1059130-1059140 chr12:1059129-1059142 chr12:1059133-1059142 chr12:1059122-1059143 chr12:1059127-1059145
23	POLR2A	chr12:1058160-1059570	GM12891	blood:	n/a	n/a
24	CEBPB	chr12:1058362-1059630	GM12878	blood:	n/a	n/a
25	FOXM1	chr12:1058472-1059620	GM12878	blood:	n/a	n/a
26	POLR2A	chr12:1057467-1059528	GM12878	blood:	n/a	n/a
27	RAD21	chr12:1058218-1059552	HCT-116	colon:	n/a	chr12:1059011-1059020 chr12:1059125-1059144 chr12:1059127-1059139 chr12:1059318-1059327 chr12:1059128-1059141 chr12:1059129-1059139
28	MAX	chr12:1058209-1059520	GM12878	blood:	n/a	n/a
29	CTCF	chr12:1058972-1059444	Medullo	brain:	n/a	chr12:1059130-1059140 chr12:1059129-1059142 chr12:1059133-1059142 chr12:1059122-1059143 chr12:1059127-1059145
30	POLR2A	chr12:1058167-1059512	PANC-1	pancreas:	n/a	n/a
31	MAX	chr12:1057914-1059535	A549	lung:	n/a	n/a
32	CTCF	chr12:1058797-1059518	K562	blood:	n/a	chr12:1059130-1059140 chr12:1059129-1059142 chr12:1059133-1059142 chr12:1059122-1059143 chr12:1059127-1059145
33	POLR2A	chr12:1058376-1059515	GM12878	blood:	n/a	n/a
34	EP300	chr12:1058506-1059520	GM12878	blood:	n/a	chr12:1059224-1059233
35	STAT5A	chr12:1058094-1059520	GM12878	blood:	n/a	chr12:1058358-1058366
36	CTCF	chr12:1058972-1059444	Gliobla	brain:	n/a	chr12:1059130-1059140 chr12:1059129-1059142 chr12:1059133-1059142 chr12:1059122-1059143 chr12:1059127-1059145
37	RAD21	chr12:1058668-1059508	A549	lung:	n/a	chr12:1059011-1059020 chr12:1059125-1059144 chr12:1059127-1059139 chr12:1059318-1059327 chr12:1059128-1059141 chr12:1059129-1059139
38	BCLAF1	chr12:1058229-1059548	GM12878	blood:	n/a	chr12:1058486-1058495
39	FOXM1	chr12:1058077-1059486	ECC-1	luminal epithelium:	n/a	n/a
40	PAX5	chr12:1058430-1059663	GM12878	blood:	n/a	n/a
41	ATF2	chr12:1058380-1059547	GM12878	blood:	n/a	n/a
42	YY1	chr12:1058126-1059548	GM12892	blood:	n/a	chr12:1058667-1058678
43	POLR2A	chr12:1058400-1059439	GM10847	blood:	n/a	n/a
44	PBX3	chr12:1059310-1059506	GM12878	blood:	n/a	n/a
45	MXI1	chr12:1058193-1059524	GM12878	blood:	n/a	n/a
46	CBX3	chr12:1058259-1059476	HCT-116	colon:	n/a	n/a
47	SIN3A	chr12:1058294-1059433	H1-hESC	embryonic stem cell:	n/a	chr12:1058901-1058914
48	RUNX3	chr12:1058281-1059634	GM12878	blood:	n/a	chr12:1059321-1059338
49	EP300	chr12:1058469-1059573	GM12878	blood:	n/a	chr12:1059224-1059233
50	REST	chr12:1059258-1059482	Hela-S3	cervix:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:861574..863792-chr12:1057514..1060138,2	K562	blood:
2	chr12:1057331..1059748-chr12:1192287..1193829,2	MCF-7	breast:
3	chr12:1057310..1059974-chr13:20532489..20534710,2	MCF-7	breast:
4	chr12:1057714..1059446-chr12:1702277..1704204,2	MCF-7	breast:
5	chr12:1058398..1059945-chr12:1134448..1137215,2	MCF-7	breast:
6	chr12:860213..861917-chr12:1056995..1059720,2	MCF-7	breast:
7	chr12:1058754..1060950-chr12:1097741..1100141,2	MCF-7	breast:
8	chr12:1056985..1060702-chr12:1098122..1101434,9	MCF-7	breast:

Variant related genes	Relation type
RAD52	TF binding region
ENSG00000121741	Chromatin interaction
ENSG00000250132	Chromatin interaction
ENSG00000082805	Chromatin interaction
ENSG00000060237	Chromatin interaction
ENSG00000171823	Chromatin interaction
ENSG00000002016	Chromatin interaction

Extended variants
information (count: 52 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs10735067	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10774473	0.99[ASN][1000 genomes]
rs10849603	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10849604	0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11064601	0.96[ASN][1000 genomes]
rs11064613	1.00[ASN][1000 genomes]
rs12231979	0.98[ASN][1000 genomes]
rs1833095	0.96[ASN][1000 genomes]
rs2887531	0.98[ASN][1000 genomes]
rs2887534	0.83[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4344554	0.99[ASN][1000 genomes]
rs4766394	0.96[ASN][1000 genomes]
rs60875507	0.96[ASN][1000 genomes]
rs6489771	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7139393	0.98[ASN][1000 genomes]
rs7294431	0.98[ASN][1000 genomes]
rs7298449	0.94[ASN][1000 genomes]
rs7306276	0.82[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs7311263	0.98[ASN][1000 genomes]
rs7314098	0.98[ASN][1000 genomes]
rs73604294	0.98[ASN][1000 genomes]
rs7960039	0.93[ASN][1000 genomes]
rs7968028	0.93[ASN][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	nsv1044433	chr12:321619-1065402	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
4	nsv541323	chr12:321619-1065402	Strong transcription Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
5	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
6	nsv556890	chr12:662448-1100555	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
7	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
8	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
9	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
10	nsv1042333	chr12:907975-1081509	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
11	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
12	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
13	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
14	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
15	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
16	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
17	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
18	nsv1041675	chr12:993822-1091354	Flanking Active TSS Strong transcription Weak transcription Enhancers Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
19	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
20	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
21	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
22	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
23	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
24	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
25	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
26	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
27	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
28	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
29	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

No data

Chromatin state (count:100 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:1057000-1059600	Active TSS	iPS-20b Cell Line	embryonic stem cell
2	chr12:1057200-1059600	Active TSS	NHLF	lung
3	chr12:1057400-1059600	Active TSS	H1 Cell Line	embryonic stem cell
4	chr12:1057400-1059600	Active TSS	HUES48 Cell Line	embryonic stem cell
5	chr12:1057400-1059600	Active TSS	HUES6 Cell Line	embryonic stem cell
6	chr12:1057400-1059600	Active TSS	iPS-15b Cell Line	embryonic stem cell
7	chr12:1057400-1059600	Active TSS	iPS-18 Cell Line	embryonic stem cell
8	chr12:1057400-1059600	Active TSS	Fetal Kidney	kidney
9	chr12:1057400-1059600	Active TSS	Psoas Muscle	Psoas
10	chr12:1057600-1059600	Active TSS	HUES64 Cell Line	embryonic stem cell
11	chr12:1057600-1059600	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
12	chr12:1057600-1059600	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr12:1057600-1059600	Active TSS	Colonic Mucosa	Colon
14	chr12:1057600-1059600	Active TSS	Pancreatic Islets	Pancreatic Islet
15	chr12:1057600-1059600	Active TSS	Rectal Smooth Muscle	rectum
16	chr12:1057800-1059600	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr12:1057800-1059600	Active TSS	H9 Cell Line	embryonic stem cell
18	chr12:1057800-1059600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr12:1057800-1059600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr12:1057800-1059600	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr12:1057800-1059600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr12:1057800-1059600	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr12:1057800-1059600	Active TSS	Brain Hippocampus Middle	brain
24	chr12:1057800-1059600	Active TSS	Brain Inferior Temporal Lobe	brain
25	chr12:1057800-1059600	Active TSS	Brain Substantia Nigra	brain
26	chr12:1057800-1059600	Active TSS	Duodenum Smooth Muscle	Duodenum
27	chr12:1057800-1059600	Active TSS	Fetal Lung	lung
28	chr12:1057800-1059600	Active TSS	Left Ventricle	heart
29	chr12:1057800-1059600	Active TSS	Sigmoid Colon	Sigmoid Colon
30	chr12:1057800-1059600	Active TSS	GM12878-XiMat	blood
31	chr12:1057800-1059600	Active TSS	HMEC	breast
32	chr12:1057800-1059600	Active TSS	HUVEC	blood vessel
33	chr12:1057800-1059600	Active TSS	NHEK	skin
34	chr12:1058000-1059600	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr12:1058000-1059600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr12:1058000-1059600	Active TSS	Brain Anterior Caudate	brain
37	chr12:1058000-1059600	Active TSS	Colon Smooth Muscle	Colon
38	chr12:1058000-1059600	Active TSS	Fetal Intestine Small	intestine
39	chr12:1058000-1059600	Active TSS	Fetal Stomach	stomach
40	chr12:1058000-1059600	Active TSS	Pancreas	Pancrea
41	chr12:1058000-1059600	Active TSS	Placenta Amnion	Placenta Amnion
42	chr12:1058000-1059600	Active TSS	Right Ventricle	heart
43	chr12:1058000-1059600	Active TSS	NH-A	brain
44	chr12:1058000-1059800	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr12:1058200-1059600	Active TSS	Breast Myoepithelial Primary Cells	Breast
46	chr12:1058200-1059600	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr12:1058200-1059600	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr12:1058200-1059600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr12:1058200-1059600	Active TSS	Brain Cingulate Gyrus	brain
50	chr12:1058200-1059600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain

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