Variant report

Variant	rs1148550
Chromosome Location	chr12:57915680-57915681
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:204)
CpG islands
(count:61)
Chromatin interactive
region (count:53)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:204 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	RAD21	chr12:57915412-57916055	HepG2	liver:	n/a	chr12:57915557-57915570
2	MAX	chr12:57915284-57916825	HepG2	liver:	n/a	chr12:57916339-57916349 chr12:57916084-57916093 chr12:57916730-57916740
3	POLR2A	chr12:57915282-57917210	GM19099	blood:	n/a	n/a
4	POLR2A	chr12:57915382-57916341	GM12891	blood:	n/a	n/a
5	POLR2A	chr12:57915317-57916843	GM12878	blood:	n/a	n/a
6	MAX	chr12:57915577-57916838	ECC-1	luminal epithelium:	n/a	chr12:57916339-57916349 chr12:57916084-57916093 chr12:57916730-57916740
7	SIN3AK20	chr12:57915540-57916587	MCF-7	breast:	n/a	n/a
8	TBL1XR1	chr12:57915372-57916761	K562	blood:	n/a	n/a
9	POLR2A	chr12:57915561-57916154	HUVEC	blood vessel:	n/a	n/a
10	TCF7L2	chr12:57915231-57916590	PANC-1	pancreas:	n/a	chr12:57916193-57916207
11	POLR2A	chr12:57915393-57917444	GM19193	blood:	n/a	n/a
12	MAX	chr12:57915660-57917188	H1-hESC	embryonic stem cell:	n/a	chr12:57916339-57916349 chr12:57916084-57916093 chr12:57916730-57916740
13	RAD21	chr12:57915400-57915699	HepG2	liver:	n/a	chr12:57915557-57915570
14	MYBL2	chr12:57915492-57916486	HepG2	liver:	n/a	n/a
15	POLR2A	chr12:57913349-57917243	Raji	blood:	n/a	n/a
16	POLR2A	chr12:57908101-57916508	PANC-1	pancreas:	n/a	n/a
17	CTCF	chr12:57915540-57915690	HEEpiC	esophagus:	n/a	n/a
18	CHD2	chr12:57915503-57917183	GM12878	blood:	n/a	n/a
19	HCFC1	chr12:57915227-57917771	Hela-S3	cervix:	n/a	n/a
20	POLR2A	chr12:57912918-57917367	GM12878	blood:	n/a	n/a
21	POLR2A	chr12:57915483-57918252	Hela-S3	cervix:	n/a	n/a
22	NR2F2	chr12:57915162-57916655	K562	blood:	n/a	chr12:57916076-57916091
23	CTCF	chr12:57915540-57915790	GM12865	blood:	n/a	n/a
24	CTCF	chr12:57915540-57915690	WERI-Rb-1	eye:	n/a	n/a
25	POLR2A	chr12:57915371-57916774	GM12891	blood:	n/a	n/a
26	MXI1	chr12:57912772-57916808	IMR90	lung:	n/a	n/a
27	REST	chr12:57915218-57917582	H1-neurons	neurons:	n/a	chr12:57916449-57916458 chr12:57915324-57915338 chr12:57916602-57916615
28	CBX3	chr12:57915347-57916407	K562	blood:	n/a	n/a
29	TBL1XR1	chr12:57915371-57916747	K562	blood:	n/a	n/a
30	RUNX3	chr12:57915590-57916620	GM12878	blood:	n/a	n/a
31	CTCF	chr12:57915296-57915720	K562	blood:	n/a	n/a
32	NR2F2	chr12:57915639-57916472	HepG2	liver:	n/a	chr12:57916076-57916091
33	USF1	chr12:57915643-57916473	HCT-116	colon:	n/a	chr12:57916082-57916093
34	FOXM1	chr12:57915631-57916523	GM12878	blood:	n/a	n/a
35	POLR2A	chr12:57911713-57919299	SK-N-MC	brain:	n/a	n/a
36	CTCF	chr12:57915640-57915790	K562	blood:	n/a	n/a
37	MAX	chr12:57915638-57916262	H1-hESC	embryonic stem cell:	n/a	chr12:57916084-57916093
38	POLR2A	chr12:57915080-57916283	GM12878	blood:	n/a	n/a
39	SIN3AK20	chr12:57915627-57916507	A549	lung:	n/a	n/a
40	POLR2A	chr12:57915158-57916797	PANC-1	pancreas:	n/a	n/a
41	TAF1	chr12:57915327-57915785	K562	blood:	n/a	n/a
42	CHD2	chr12:57915410-57916778	HepG2	liver:	n/a	n/a
43	KAP1	chr12:57915369-57916257	HEK293	kidney:	n/a	n/a
44	HEY1	chr12:57914555-57915702	K562	blood:	n/a	n/a
45	BHLHE40	chr12:57915449-57916596	K562	blood:	n/a	n/a
46	HEY1	chr12:57914593-57916521	K562	blood:	n/a	n/a
47	POLR2A	chr12:57915482-57917176	GM12892	blood:	n/a	n/a
48	POLR2A	chr12:57914580-57916523	GM12878	blood:	n/a	n/a
49	POLR2A	chr12:57915334-57916341	GM12892	blood:	n/a	n/a
50	ELK1	chr12:57915635-57916361	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:57915636-57915686	MCF-7	breast:	n/a
2	chr12:57915636-57915686	HPAEpiC	pulmonary alveolar:	n/a
3	chr12:57915636-57915686	AG09309	skin:	n/a
4	chr12:57915636-57915686	SKMC	muscle:	n/a
5	chr12:57915636-57915686	HCF	heart:	n/a
6	chr12:57915636-57915686	HNPCEpiC	eye:	n/a
7	chr12:57915636-57915686	Hepatocyte	liver:	n/a
8	chr12:57915636-57915686	AG09319	gingival:	n/a
9	chr12:57915636-57915686	ProgFib	skin:	n/a
10	chr12:57915636-57915686	HAEpiC	amniotic membrane:	n/a
11	chr12:57915636-57915686	HCM	heart:	n/a
12	chr12:57915636-57915686	Caco-2	colon:	n/a
13	chr12:57915636-57915686	Jurkat	blood:	n/a
14	chr12:57915636-57915686	GM12878	blood:	n/a
15	chr12:57915636-57915686	PFSK-1	brain:	n/a
16	chr12:57915636-57915686	BJ	skin:	n/a
17	chr12:57915636-57915686	NHBE	bronchial:	n/a
18	chr12:57915636-57915686	NH-A	brain:	n/a
19	chr12:57915636-57915686	GM12892	blood:	n/a
20	chr12:57915636-57915686	HMEC	breast:	n/a
21	chr12:57915636-57915686	HepG2	liver:	n/a
22	chr12:57915636-57915686	HEK293	kidney:	embryo
23	chr12:57915636-57915686	ECC-1	luminal epithelium:	n/a
24	chr12:57915636-57915686	H1-hESC	embryonic stem cell:	embryo
25	chr12:57915636-57915686	NT2-D1	testis:	n/a
26	chr12:57915636-57915686	CMK	blood:	n/a
27	chr12:57915636-57915686	NB4	blood:	n/a
28	chr12:57915636-57915686	HRCEpiC	kidney:	n/a
29	chr12:57915636-57915686	MCF10A-Er-Src	breast:	n/a
30	chr12:57915636-57915686	SAEC	small airway:	n/a
31	chr12:57915636-57915686	HRE	kidney:	n/a
32	chr12:57915636-57915686	AoSMC	blood vessel:	n/a
33	chr12:57915636-57915686	PANC-1	pancreas:	n/a
34	chr12:57915636-57915686	K562	blood:	n/a
35	chr12:57915636-57915686	RPTEC	kidney:	n/a
36	chr12:57915636-57915686	HRPEpiC	eye:	n/a
37	chr12:57915636-57915686	SK-N-SH_RA	brain:	n/a
38	chr12:57915636-57915686	PrEC	prostate:	n/a
39	chr12:57915636-57915686	HL-60	blood:	n/a
40	chr12:57915636-57915686	HEEpiC	esophagus:	n/a
41	chr12:57915636-57915686	GM12891	blood:	n/a
42	chr12:57915636-57915686	LNCaP	prostate:	n/a
43	chr12:57915636-57915686	HIPEpiC	eye:	n/a
44	chr12:57915636-57915686	GM06990	blood:	n/a
45	chr12:57915636-57915686	BE2_C	brain:	n/a
46	chr12:57915636-57915686	ovcar-3	ovarian:	n/a
47	chr12:57915636-57915686	AG04450	lung:	fetal
48	chr12:57915636-57915686	AG10803	skin:	n/a
49	chr12:57915636-57915686	NHDF-neo	bronchial:	n/a
50	chr12:57915636-57915686	HCPEpiC	choroid plexus:	n/a

(count:53 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr12:57117159..57119489-chr12:57914533..57916753,2	K562	blood:
2	chr12:57911911..57916321-chr12:58013702..58018076,7	K562	blood:
3	chr12:57912814..57915992-chr12:58164344..58170030,6	K562	blood:
4	chr12:57912789..57915911-chr12:58119258..58122771,4	MCF-7	breast:
5	chr12:57879207..57888227-chr12:57906247..57918451,36	K562	blood:
6	chr12:57849885..57859254-chr12:57908711..57915821,16	K562	blood:
7	chr12:57913785..57915861-chr12:58131130..58132834,2	MCF-7	breast:
8	chr12:57915553..57917499-chr12:58144787..58147876,3	K562	blood:
9	chr12:57914271..57916098-chr12:58131440..58134732,4	K562	blood:
10	chr12:57909973..57915898-chr12:58127755..58134567,15	K562	blood:
11	chr12:57913428..57916180-chr12:58009743..58011363,2	MCF-7	breast:
12	chr12:57915482..57918597-chr12:58119014..58121092,3	MCF-7	breast:
13	chr12:57913580..57915686-chr3:186500312..186502115,2	K562	blood:
14	chr12:57908910..57916122-chr12:58022622..58031573,17	K562	blood:
15	chr12:57913372..57915977-chr12:58164344..58168645,6	K562	blood:
16	chr12:57914544..57916510-chr12:58137621..58139842,2	MCF-7	breast:
17	chr12:57481972..57484968-chr12:57912943..57915711,3	K562	blood:
18	chr12:57914556..57917935-chr12:58138142..58139921,3	K562	blood:
19	chr12:57915284..57917737-chr12:58135302..58137824,2	K562	blood:
20	chr12:57913753..57916510-chr12:57996799..57998980,2	MCF-7	breast:
21	chr12:57890108..57896575-chr12:57912675..57917509,9	MCF-7	breast:
22	chr12:57914171..57915978-chr17:7477098..7479787,2	K562	blood:
23	chr12:57911754..57916322-chr12:58006406..58010716,5	K562	blood:
24	chr12:57852034..57858739-chr12:57911478..57917144,8	MCF-7	breast:
25	chr12:57822673..57825673-chr12:57914537..57916745,4	K562	blood:
26	chr12:57913915..57915790-chr12:58160271..58161971,2	K562	blood:
27	chr12:57912625..57916215-chr12:58016074..58021603,6	K562	blood:
28	chr12:57913857..57916876-chr12:58140485..58143986,3	K562	blood:
29	chr12:57082052..57084048-chr12:57915298..57917787,2	K562	blood:
30	chr12:57850154..57858218-chr12:57910899..57919538,20	K562	blood:
31	chr12:57915543..57917497-chr12:58086337..58088295,2	K562	blood:
32	chr12:57914619..57916153-chr12:57984112..57986210,2	K562	blood:
33	chr12:57912759..57917021-chr12:58137187..58141030,5	MCF-7	breast:
34	chr12:57480746..57483234-chr12:57915069..57916762,2	MCF-7	breast:
35	chr12:57914860..57917603-chr12:58144909..58148802,3	K562	blood:
36	chr12:57912866..57916321-chr12:58013594..58015753,4	K562	blood:
37	chr12:57911699..57918406-chr12:58000825..58010019,18	K562	blood:
38	chr12:57889487..57901620-chr12:57907600..57919310,30	K562	blood:
39	chr12:57914797..57916581-chr12:58144797..58147078,2	MCF-7	breast:
40	chr12:57912818..57918945-chr12:58145879..58149998,6	MCF-7	breast:
41	chr12:57482455..57482983-chr12:57915647..57916484,3	MCF-7	breast:
42	chr12:57880356..57884964-chr12:57910434..57915758,10	MCF-7	breast:
43	chr12:57633994..57636075-chr12:57915508..57917447,2	MCF-7	breast:
44	chr12:57622307..57625065-chr12:57914079..57916302,2	K562	blood:
45	chr12:57912826..57917389-chr12:58135038..58139778,7	K562	blood:
46	chr12:57879869..57888452-chr12:57905809..57918310,36	K562	blood:
47	chr12:57881044..57886958-chr12:57910925..57918058,16	MCF-7	breast:
48	chr12:57022647..57024200-chr12:57914348..57917342,2	MCF-7	breast:
49	chr12:57913089..57916136-chr12:58086816..58089656,3	MCF-7	breast:
50	chr12:57908910..57916403-chr12:58022622..58028885,15	K562	blood:

No data

Variant related genes	Relation type
MIR616	TF binding region
MBD6	TF binding region
DDIT3	TF binding region
DDIT3	CpG island
MBD6	CpG island
MIR616	CpG island
ENSG00000135502	Chromatin interaction
ENSG00000182199	Chromatin interaction
ENSG00000161960	Chromatin interaction
ENSG00000209582	Chromatin interaction
ENSG00000166908	Chromatin interaction
ENSG00000123329	Chromatin interaction
ENSG00000257921	Chromatin interaction
ENSG00000266465	Chromatin interaction
ENSG00000224713	Chromatin interaction
ENSG00000139266	Chromatin interaction
ENSG00000123427	Chromatin interaction
ENSG00000166986	Chromatin interaction
ENSG00000135454	Chromatin interaction
ENSG00000166886	Chromatin interaction
ENSG00000111012	Chromatin interaction
ENSG00000166881	Chromatin interaction
ENSG00000076108	Chromatin interaction
ENSG00000179912	Chromatin interaction
ENSG00000257698	Chromatin interaction
ENSG00000110958	Chromatin interaction
ENSG00000135446	Chromatin interaction
ENSG00000263826	Chromatin interaction
ENSG00000240771	Chromatin interaction
ENSG00000156976	Chromatin interaction
ENSG00000178498	Chromatin interaction
ENSG00000037897	Chromatin interaction
ENSG00000258001	Chromatin interaction
ENSG00000111087	Chromatin interaction
ENSG00000196531	Chromatin interaction
ENSG00000135452	Chromatin interaction
ENSG00000255737	Chromatin interaction
ENSG00000185633	Chromatin interaction
ENSG00000135506	Chromatin interaction
ENSG00000257499	Chromatin interaction
ENSG00000135439	Chromatin interaction

Extended variants
information (count: 27 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1284467	1.00[ASW][hapmap];1.00[EUR][1000 genomes]
rs1679366	1.00[EUR][1000 genomes]
rs2620680	1.00[ASW][hapmap];1.00[EUR][1000 genomes]
rs537161	0.82[ASW][hapmap];1.00[EUR][1000 genomes]
rs59235552	1.00[EUR][1000 genomes]
rs60374392	1.00[EUR][1000 genomes]
rs703833	1.00[EUR][1000 genomes]
rs703840	1.00[EUR][1000 genomes]
rs775325	1.00[EUR][1000 genomes]
rs776340	1.00[EUR][1000 genomes]
rs7973639	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv899117	chr12:57811414-57926472	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	103 gene(s)	inside rSNPs	diseases
2	nsv899118	chr12:57811414-57946477	Weak transcription Strong transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	106 gene(s)	inside rSNPs	diseases
3	esv1812398	chr12:57829733-58001868	Flanking Active TSS Active TSS Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
4	esv2758310	chr12:57829733-58001868	Active TSS Genic enhancers Enhancers Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
5	esv2759901	chr12:57829733-58001868	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
6	nsv428283	chr12:57829733-58001868	Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh Weak transcription Enhancers Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
7	nsv469411	chr12:57844049-57921188	Active TSS Flanking Active TSS Strong transcription Weak transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	89 gene(s)	inside rSNPs	diseases
8	nsv559032	chr12:57844049-57921188	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	89 gene(s)	inside rSNPs	diseases
9	nsv559033	chr12:57848639-57946477	Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS Enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
10	nsv899119	chr12:57851182-57923451	Strong transcription Flanking Active TSS Active TSS Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	89 gene(s)	inside rSNPs	diseases
11	nsv559034	chr12:57859932-58012233	Strong transcription Weak transcription Flanking Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	89 gene(s)	inside rSNPs	diseases
12	nsv1038741	chr12:57877355-58174506	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	126 gene(s)	inside rSNPs	diseases
13	nsv541503	chr12:57877355-58174506	Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	126 gene(s)	inside rSNPs	diseases
14	nsv899120	chr12:57886609-57921188	Active TSS Genic enhancers Weak transcription Strong transcription Flanking Active TSS Enhancers 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 miRNA target site	72 gene(s)	inside rSNPs	diseases
15	nsv559036	chr12:57911212-57916042	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA	68 gene(s)	inside rSNPs	n/a
16	esv3429239	chr12:57915210-57918058	Active TSS Flanking Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	41 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:57912000-57917600	Active TSS	Psoas Muscle	Psoas
2	chr12:57912400-57918600	Active TSS	Pancreatic Islets	Pancreatic Islet
3	chr12:57912800-57915800	Active TSS	H9 Cell Line	embryonic stem cell
4	chr12:57913800-57917400	Active TSS	ES-I3 Cell Line	embryonic stem cell
5	chr12:57914200-57916000	Weak transcription	Small Intestine	intestine
6	chr12:57914400-57915800	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr12:57914400-57916000	Weak transcription	Gastric	stomach
8	chr12:57914400-57916000	Weak transcription	Ovary	ovary
9	chr12:57914600-57916200	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr12:57914600-57916200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
11	chr12:57914600-57916200	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr12:57914600-57916400	Flanking Active TSS	Primary T cells fromperipheralblood	blood
13	chr12:57914600-57916400	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
14	chr12:57914600-57916400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr12:57914600-57916400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr12:57914600-57916400	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
17	chr12:57914800-57916000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr12:57914800-57916200	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr12:57914800-57916200	Flanking Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
20	chr12:57914800-57916200	Flanking Active TSS	Primary B cells from cord blood	blood
21	chr12:57914800-57916200	Flanking Active TSS	Primary T cells from cord blood	blood
22	chr12:57914800-57916200	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
23	chr12:57914800-57916200	Flanking Active TSS	Adipose Nuclei	Adipose
24	chr12:57914800-57916200	Flanking Active TSS	Brain Hippocampus Middle	brain
25	chr12:57914800-57916200	Flanking Active TSS	Colon Smooth Muscle	Colon
26	chr12:57914800-57916200	Flanking Active TSS	Fetal Heart	heart
27	chr12:57914800-57916200	Flanking Active TSS	Rectal Smooth Muscle	rectum
28	chr12:57914800-57916200	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
29	chr12:57914800-57916200	Flanking Active TSS	K562	blood
30	chr12:57914800-57916400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
31	chr12:57914800-57916400	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
32	chr12:57914800-57916400	Flanking Active TSS	Fetal Intestine Large	intestine
33	chr12:57914800-57916400	Flanking Active TSS	Stomach Smooth Muscle	stomach
34	chr12:57914800-57916400	Flanking Active TSS	Dnd41	blood
35	chr12:57914800-57916400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
36	chr12:57915000-57915800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr12:57915000-57915800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr12:57915000-57915800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr12:57915000-57915800	Enhancers	Primary monocytes fromperipheralblood	blood
40	chr12:57915000-57915800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
41	chr12:57915000-57915800	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
42	chr12:57915000-57915800	Enhancers	Fetal Stomach	stomach
43	chr12:57915000-57915800	Enhancers	Fetal Thymus	thymus
44	chr12:57915000-57915800	Enhancers	Left Ventricle	heart
45	chr12:57915000-57915800	Enhancers	Lung	lung
46	chr12:57915000-57915800	Enhancers	Pancreas	Pancrea
47	chr12:57915000-57915800	Enhancers	Right Atrium	heart
48	chr12:57915000-57915800	Enhancers	Right Ventricle	heart
49	chr12:57915000-57915800	Enhancers	HSMM	muscle
50	chr12:57915000-57915800	Enhancers	HUVEC	blood vessel

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