Variant report

Variant	rs11571379
Chromosome Location	chr12:1059143-1059144
allele	C/T
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	CTCF	chr12:1059060-1059210	HBMEC	blood vessel:	n/a	chr12:1059130-1059140 chr12:1059129-1059142 chr12:1059133-1059142 chr12:1059122-1059143 chr12:1059127-1059145
2	YY1	chr12:1058132-1059550	H1-hESC	embryonic stem cell:	n/a	chr12:1058667-1058678
3	CTCF	chr12:1058977-1059439	K562	blood:	n/a	chr12:1059130-1059140 chr12:1059129-1059142 chr12:1059133-1059142 chr12:1059122-1059143 chr12:1059127-1059145
4	POLR2A	chr12:1058170-1059368	U87	brain:	n/a	n/a
5	ELF1	chr12:1058543-1059293	HepG2	liver:	n/a	chr12:1058688-1058697 chr12:1058687-1058698
6	FOXA1	chr12:1058503-1059180	HepG2	liver:	n/a	n/a
7	CTCF	chr12:1059060-1059210	AG09319	gingival:	n/a	chr12:1059130-1059140 chr12:1059129-1059142 chr12:1059133-1059142 chr12:1059122-1059143 chr12:1059127-1059145
8	ATF3	chr12:1058769-1059190	GM12878	blood:	n/a	n/a
9	CTCF	chr12:1058959-1059478	GM19240	blood:	n/a	chr12:1059130-1059140 chr12:1059129-1059142 chr12:1059133-1059142 chr12:1059122-1059143 chr12:1059127-1059145
10	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
11	RAD21	chr12:1058875-1059280	K562	blood:	n/a	chr12:1059011-1059020 chr12:1059125-1059144 chr12:1059127-1059139 chr12:1059128-1059141 chr12:1059129-1059139
12	POLR2A	chr12:1058985-1059157	A549	lung:	n/a	n/a
13	POLR2A	chr12:1057717-1059641	GM12892	blood:	n/a	n/a
14	MAX	chr12:1058097-1059555	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTCF	chr12:1059080-1059230	GM12875	blood:	n/a	chr12:1059130-1059140 chr12:1059129-1059142 chr12:1059133-1059142 chr12:1059122-1059143 chr12:1059127-1059145
16	KAP1	chr12:1058222-1059211	HEK293	kidney:	n/a	n/a
17	FOXA2	chr12:1058572-1059244	A549	lung:	n/a	n/a
18	ELF1	chr12:1058232-1059636	GM12878	blood:	n/a	chr12:1058688-1058697 chr12:1058687-1058698
19	GABPA	chr12:1058514-1059268	SK-N-SH	brain:	n/a	n/a
20	CTCF	chr12:1058998-1059377	MCF-7	breast:	n/a	chr12:1059130-1059140 chr12:1059129-1059142 chr12:1059133-1059142 chr12:1059122-1059143 chr12:1059127-1059145
21	ZKSCAN1	chr12:1058452-1059311	Hela-S3	cervix:	n/a	n/a
22	EP300	chr12:1058650-1059332	T-47D	breast:	n/a	chr12:1059224-1059233
23	RCOR1	chr12:1058445-1059203	K562	blood:	n/a	n/a
24	POLR2A	chr12:1057361-1059459	GM12891	blood:	n/a	n/a
25	ATF3	chr12:1058603-1059472	H1-hESC	embryonic stem cell:	n/a	n/a
26	ZNF384	chr12:1058552-1059422	GM12878	blood:	n/a	n/a
27	EBF1	chr12:1058990-1059636	GM12878	blood:	n/a	chr12:1059446-1059457
28	STAT3	chr12:1058738-1059259	MCF10A-Er-Src	breast:	n/a	n/a
29	CTCF	chr12:1059060-1059210	HA-sp	spinal cord:	n/a	chr12:1059130-1059140 chr12:1059129-1059142 chr12:1059133-1059142 chr12:1059122-1059143 chr12:1059127-1059145
30	CTCF	chr12:1059000-1059150	WI-38	lung:	n/a	chr12:1059130-1059140 chr12:1059129-1059142 chr12:1059133-1059142 chr12:1059122-1059143 chr12:1059127-1059145
31	CEBPB	chr12:1058936-1059264	GM12878	blood:	n/a	n/a
32	POLR2A	chr12:1058241-1059245	PFSK-1	brain:	n/a	n/a
33	ZEB1	chr12:1059044-1059247	GM12878	blood:	n/a	n/a
34	POLR2A	chr12:1058160-1059613	H1-hESC	embryonic stem cell:	n/a	n/a
35	MAX	chr12:1058057-1059290	A549	lung:	n/a	n/a
36	RXRA	chr12:1059016-1059172	GM12878	blood:	n/a	chr12:1059125-1059145 chr12:1059071-1059078
37	CREB1	chr12:1058136-1059516	A549	lung:	n/a	n/a
38	CTCF	chr12:1059040-1059190	GM12866	blood:	n/a	chr12:1059130-1059140 chr12:1059129-1059142 chr12:1059133-1059142 chr12:1059122-1059143 chr12:1059127-1059145
39	MBD4	chr12:1058598-1059331	HepG2	liver:	n/a	n/a
40	EP300	chr12:1058555-1059554	GM12878	blood:	n/a	chr12:1059224-1059233
41	POLR2A	chr12:1058195-1059511	H1-hESC	embryonic stem cell:	n/a	n/a
42	POLR2A	chr12:1057952-1059583	GM12892	blood:	n/a	n/a
43	ZNF143	chr12:1058184-1059535	GM12878	blood:	n/a	chr12:1058380-1058399
44	CEBPB	chr12:1058971-1059301	A549	lung:	n/a	n/a
45	EP300	chr12:1058151-1059373	A549	lung:	n/a	chr12:1058359-1058368 chr12:1059224-1059233
46	POLR2A	chr12:1058079-1059452	GM12878	blood:	n/a	n/a
47	POLR2A	chr12:1057915-1059530	HL-60	blood:	n/a	n/a
48	PML	chr12:1058542-1059220	MCF-7	breast:	n/a	n/a
49	E2F4	chr12:1058579-1059306	Hela-S3	cervix:	n/a	chr12:1059086-1059098 chr12:1059085-1059096 chr12:1059015-1059024
50	RCOR1	chr12:1058183-1059620	GM12878	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:861574..863792-chr12:1057514..1060138,2	K562	blood:
2	chr12:1058342..1059150-chr5:172197582..172198243,2	Hela-S3	cervix:
3	chr12:1057331..1059748-chr12:1192287..1193829,2	MCF-7	breast:
4	chr12:1057310..1059974-chr13:20532489..20534710,2	MCF-7	breast:
5	chr11:62608653..62609618-chr12:1058386..1059229,2	Hela-S3	cervix:
6	chr12:1057714..1059446-chr12:1702277..1704204,2	MCF-7	breast:
7	chr12:1058398..1059945-chr12:1134448..1137215,2	MCF-7	breast:
8	chr12:1058395..1059394-chr15:40856943..40857497,2	Hela-S3	cervix:
9	chr12:860213..861917-chr12:1056995..1059720,2	MCF-7	breast:
10	chr12:1058754..1060950-chr12:1097741..1100141,2	MCF-7	breast:
11	chr12:1056985..1060702-chr12:1098122..1101434,9	MCF-7	breast:

Variant related genes	Relation type
RAD52	TF binding region
ENSG00000002016	Chromatin interaction
ENSG00000082805	Chromatin interaction
ENSG00000250132	Chromatin interaction
ENSG00000060237	Chromatin interaction
ENSG00000120129	Chromatin interaction
ENSG00000121741	Chromatin interaction
ENSG00000171823	Chromatin interaction
ENSG00000128891	Chromatin interaction
ENSG00000133316	Chromatin interaction

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs10849601	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10849602	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10849605	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11064598	0.81[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs11064607	0.81[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs11064614	0.92[ASN][1000 genomes]
rs11571378	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3748522	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs55791720	0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs59943404	0.97[ASN][1000 genomes]
rs7302558	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:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:1057000-1059600	Active TSS	iPS-20b Cell Line	embryonic stem cell
2	chr12:1057200-1059400	Active TSS	ES-I3 Cell Line	embryonic stem cell
3	chr12:1057200-1059400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr12:1057200-1059600	Active TSS	NHLF	lung
5	chr12:1057400-1059600	Active TSS	H1 Cell Line	embryonic stem cell
6	chr12:1057400-1059600	Active TSS	HUES48 Cell Line	embryonic stem cell
7	chr12:1057400-1059600	Active TSS	HUES6 Cell Line	embryonic stem cell
8	chr12:1057400-1059600	Active TSS	iPS-15b Cell Line	embryonic stem cell
9	chr12:1057400-1059600	Active TSS	iPS-18 Cell Line	embryonic stem cell
10	chr12:1057400-1059600	Active TSS	Fetal Kidney	kidney
11	chr12:1057400-1059600	Active TSS	Psoas Muscle	Psoas
12	chr12:1057600-1059200	Active TSS	Rectal Mucosa Donor 31	rectum
13	chr12:1057600-1059400	Active TSS	HSMM	muscle
14	chr12:1057600-1059400	Active TSS	NHDF-Ad	bronchial
15	chr12:1057600-1059600	Active TSS	HUES64 Cell Line	embryonic stem cell
16	chr12:1057600-1059600	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
17	chr12:1057600-1059600	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr12:1057600-1059600	Active TSS	Colonic Mucosa	Colon
19	chr12:1057600-1059600	Active TSS	Pancreatic Islets	Pancreatic Islet
20	chr12:1057600-1059600	Active TSS	Rectal Smooth Muscle	rectum
21	chr12:1057800-1059200	Active TSS	Primary T regulatory cells fromperipheralblood	blood
22	chr12:1057800-1059200	Active TSS	Brain Angular Gyrus	brain
23	chr12:1057800-1059200	Active TSS	Duodenum Mucosa	Duodenum
24	chr12:1057800-1059200	Active TSS	Rectal Mucosa Donor 29	rectum
25	chr12:1057800-1059200	Active TSS	A549	lung
26	chr12:1057800-1059200	Active TSS	HSMMtube	muscle
27	chr12:1057800-1059400	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr12:1057800-1059400	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
29	chr12:1057800-1059400	Active TSS	Muscle Satellite Cultured Cells	--
30	chr12:1057800-1059400	Active TSS	Hela-S3	cervix
31	chr12:1057800-1059400	Active TSS	HepG2	liver
32	chr12:1057800-1059600	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr12:1057800-1059600	Active TSS	H9 Cell Line	embryonic stem cell
34	chr12:1057800-1059600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr12:1057800-1059600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr12:1057800-1059600	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr12:1057800-1059600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr12:1057800-1059600	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr12:1057800-1059600	Active TSS	Brain Hippocampus Middle	brain
40	chr12:1057800-1059600	Active TSS	Brain Inferior Temporal Lobe	brain
41	chr12:1057800-1059600	Active TSS	Brain Substantia Nigra	brain
42	chr12:1057800-1059600	Active TSS	Duodenum Smooth Muscle	Duodenum
43	chr12:1057800-1059600	Active TSS	Fetal Lung	lung
44	chr12:1057800-1059600	Active TSS	Left Ventricle	heart
45	chr12:1057800-1059600	Active TSS	Sigmoid Colon	Sigmoid Colon
46	chr12:1057800-1059600	Active TSS	GM12878-XiMat	blood
47	chr12:1057800-1059600	Active TSS	HMEC	breast
48	chr12:1057800-1059600	Active TSS	HUVEC	blood vessel
49	chr12:1057800-1059600	Active TSS	NHEK	skin
50	chr12:1058000-1059200	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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