Variant report

Variant	rs3759115
Chromosome Location	chr12:123464279-123464280
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:70)
CpG islands
(count:0)
Chromatin interactive
region (count:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:70 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr12:123464102-123465599	GM12878	blood:	n/a	n/a
2	POLR2A	chr12:123464222-123465817	GM12892	blood:	n/a	n/a
3	POLR2A	chr12:123462700-123467376	HepG2	liver:	n/a	n/a
4	STAT5A	chr12:123464172-123465574	GM12878	blood:	n/a	n/a
5	POLR2A	chr12:123458534-123466263	K562	blood:	n/a	n/a
6	POLR2A	chr12:123462020-123470019	SK-N-MC	brain:	n/a	n/a
7	POLR2A	chr12:123464066-123466242	H1-hESC	embryonic stem cell:	n/a	n/a
8	POLR2A	chr12:123464052-123465686	U87	brain:	n/a	n/a
9	POLR2A	chr12:123464053-123464445	A549	lung:	n/a	n/a
10	JUN	chr12:123464240-123465710	K562	blood:	n/a	chr12:123464872-123464882 chr12:123464872-123464882 chr12:123464872-123464882 chr12:123464869-123464880 chr12:123464873-123464881
11	POLR2A	chr12:123464276-123466236	HUVEC	blood vessel:	n/a	n/a
12	BCL3	chr12:123463944-123465539	A549	lung:	n/a	n/a
13	POLR2A	chr12:123464006-123466178	GM12878	blood:	n/a	n/a
14	POLR2A	chr12:123463966-123465607	GM12891	blood:	n/a	n/a
15	POLR2A	chr12:123464274-123466060	GM19099	blood:	n/a	n/a
16	POLR2A	chr12:123464118-123465845	GM15510	blood:	n/a	n/a
17	POLR2A	chr12:123464224-123466005	MCF10A-Er-Src	breast:	n/a	n/a
18	POLR2A	chr12:123464191-123464535	Hela-S3	cervix:	n/a	n/a
19	POLR2A	chr12:123464048-123465976	MCF-7	breast:	n/a	n/a
20	TCF12	chr12:123463846-123466004	A549	lung:	n/a	n/a
21	POLR2A	chr12:123464088-123466135	Raji	blood:	n/a	n/a
22	POLR2A	chr12:123464199-123465877	HCT-116	colon:	n/a	n/a
23	POLR2A	chr12:123464244-123466110	GM18505	blood:	n/a	n/a
24	POLR2A	chr12:123464215-123465986	GM18951	blood:	n/a	n/a
25	POLR2A	chr12:123463929-123465785	HepG2	liver:	n/a	n/a
26	POLR2A	chr12:123463985-123466171	U87	brain:	n/a	n/a
27	POLR2A	chr12:123463935-123465551	K562	blood:	n/a	n/a
28	POLR2A	chr12:123463863-123469964	PFSK-1	brain:	n/a	n/a
29	POLR2A	chr12:123460287-123466106	K562	blood:	n/a	n/a
30	POLR2A	chr12:123463987-123465698	HUVEC	blood vessel:	n/a	n/a
31	CREB1	chr12:123464217-123466004	HepG2	liver:	n/a	n/a
32	POLR2A	chr12:123464255-123464516	ProgFib	skin:	n/a	n/a
33	POLR2A	chr12:123463967-123465853	GM12891	blood:	n/a	n/a
34	POLR2A	chr12:123464163-123465800	NB4	blood:	n/a	n/a
35	POLR2A	chr12:123463573-123466152	GM12892	blood:	n/a	n/a
36	POLR2A	chr12:123463985-123466477	U87	brain:	n/a	n/a
37	BCL3	chr12:123464265-123465507	A549	lung:	n/a	n/a
38	POLR2A	chr12:123462777-123467143	HL-60	blood:	n/a	n/a
39	POLR2A	chr12:123464136-123466124	GM19193	blood:	n/a	n/a
40	POLR2A	chr12:123463131-123465669	PANC-1	pancreas:	n/a	n/a
41	POLR2A	chr12:123462997-123465931	HL-60	blood:	n/a	n/a
42	POLR2A	chr12:123463892-123465770	GM12878	blood:	n/a	n/a
43	POLR2A	chr12:123463382-123465907	PANC-1	pancreas:	n/a	n/a
44	POLR2A	chr12:123463996-123465622	SK-N-SH	brain:	n/a	n/a
45	POLR2A	chr12:123464101-123465594	GM12878	blood:	n/a	n/a
46	POLR2A	chr12:123464052-123465681	U87	brain:	n/a	n/a
47	POLR2A	chr12:123463577-123466137	GM12878	blood:	n/a	n/a
48	POLR2A	chr12:123463395-123466020	GM12892	blood:	n/a	n/a
49	POLR2A	chr12:123464126-123464739	GM12891	blood:	n/a	n/a
50	ELF1	chr12:123463954-123466088	GM12878	blood:	n/a	n/a

No data

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:123464088..123467689-chr12:123493302..123498202,6	MCF-7	breast:
2	chr12:123374002..123376738-chr12:123462505..123465359,2	MCF-7	breast:
3	chr12:123463846..123466792-chr12:123754381..123757110,2	MCF-7	breast:
4	chr12:123463020..123465729-chr8:144897399..144899453,2	MCF-7	breast:
5	chr12:123463900..123467066-chr12:123633750..123636695,4	K562	blood:
6	chr12:123462407..123464564-chr12:123506369..123507907,2	MCF-7	breast:
7	chr12:123463187..123465154-chr12:123754619..123756805,2	K562	blood:
8	chr12:123463900..123466022-chr12:123633750..123636695,4	K562	blood:
9	chr12:123009242..123011639-chr12:123463173..123465225,2	K562	blood:
10	chr12:123317692..123320507-chr12:123463597..123466562,3	MCF-7	breast:
11	chr12:123345343..123346928-chr12:123463907..123466458,2	MCF-7	breast:
12	chr12:123463210..123468211-chr12:123716151..123721062,7	MCF-7	breast:
13	chr12:123463143..123466030-chr12:123559790..123563075,3	MCF-7	breast:
14	chr12:123318837..123320791-chr12:123463752..123466824,3	MCF-7	breast:

No data

Variant related genes	Relation type
ABCB9	TF binding region
ARL6IP4	TF binding region
ENSG00000139722	Chromatin interaction
ENSG00000111328	Chromatin interaction
ENSG00000265526	Chromatin interaction
ENSG00000130787	Chromatin interaction
ENSG00000111011	Chromatin interaction
ENSG00000130921	Chromatin interaction
ENSG00000090975	Chromatin interaction
ENSG00000051825	Chromatin interaction
ENSG00000180900	Chromatin interaction

Extended variants
information (count: 46 )
Associated
traits (count: 10 )

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs1051434	0.96[CEU][hapmap];0.82[CHB][hapmap];0.95[MEX][hapmap];0.97[TSI][hapmap];1.00[YRI][hapmap]
rs10773921	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];0.86[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10848428	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];0.86[GIH][hapmap];0.86[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap]
rs11060853	0.82[CHD][hapmap];0.95[JPT][hapmap];0.85[ASN][1000 genomes]
rs11608811	0.90[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.86[GIH][hapmap];0.95[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11613937	0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12425009	0.90[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.84[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12425850	1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1615350	0.83[ASW][hapmap];0.83[CHB][hapmap];0.82[TSI][hapmap]
rs1727293	1.00[ASW][hapmap];0.96[CEU][hapmap];0.91[CHB][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.95[MKK][hapmap];0.97[TSI][hapmap];1.00[YRI][hapmap]
rs1727295	0.91[CEU][hapmap];0.95[CHB][hapmap];1.00[YRI][hapmap]
rs1727302	0.83[CHB][hapmap];0.82[TSI][hapmap]
rs1727307	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];0.86[GIH][hapmap];0.86[JPT][hapmap];1.00[TSI][hapmap]
rs1790094	0.90[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];0.86[GIH][hapmap];0.86[JPT][hapmap];1.00[LWK][hapmap];0.95[MEX][hapmap];0.98[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap]
rs1790106	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];0.86[GIH][hapmap];0.86[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap]
rs1790121	0.90[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];0.86[GIH][hapmap];0.86[JPT][hapmap];0.91[LWK][hapmap];1.00[MEX][hapmap];0.89[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap]
rs1984658	0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs28755851	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3741530	1.00[CEU][hapmap];1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3897102	1.00[CHB][hapmap];0.95[JPT][hapmap];0.98[ASN][1000 genomes]
rs4148862	0.80[EUR][1000 genomes]
rs4148863	0.90[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];0.86[GIH][hapmap];0.86[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.80[EUR][1000 genomes]
rs4148866	0.84[CHD][hapmap];0.90[JPT][hapmap];0.84[ASN][1000 genomes]
rs4275659	1.00[ASW][hapmap];1.00[CEU][hapmap];0.95[CHB][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.93[MKK][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs55742290	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs61955196	0.84[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs61955214	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7135296	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.96[MEX][hapmap];0.98[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7296418	0.91[CEU][hapmap];0.95[CHB][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.97[TSI][hapmap];0.80[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7305511	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7957096	1.00[CEU][hapmap];0.91[CHB][hapmap];0.95[JPT][hapmap];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs883562	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs884956	1.00[ASW][hapmap];0.95[CHB][hapmap];0.90[LWK][hapmap];0.91[MEX][hapmap];0.97[MKK][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs949143	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];0.86[GIH][hapmap];0.86[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3388790	chr12:123275902-123655103	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
2	nsv899572	chr12:123292503-123477311	Active TSS Strong transcription Enhancers Flanking Active TSS Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
3	nsv899573	chr12:123312051-123528405	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
4	nsv517200	chr12:123312051-123654498	Strong transcription Weak transcription Flanking Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
5	nsv899576	chr12:123335527-123528405	Enhancers Genic enhancers Flanking Active TSS Strong transcription Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
6	nsv832532	chr12:123395927-123573137	Weak transcription Strong transcription Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
7	nsv832533	chr12:123395927-123589290	Enhancers Genic enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
8	nsv427924	chr12:123412172-123722059	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers 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	78 gene(s)	inside rSNPs	diseases
9	nsv455732	chr12:123427573-123574838	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
10	nsv560492	chr12:123427573-123574838	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
11	nsv899577	chr12:123435248-123484474	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
12	nsv899578	chr12:123459005-123474529	Enhancers Transcr. at gene 5' and 3' Active TSS Weak transcription Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases

mRNA abundance (count:10)

SNP	Gene	Cis/trans	Tissue	Source
rs3759115	SBNO1	Cis_1M	lymphoblastoid	RTeQTL
rs3759115	TMEM120B	cis	parietal	SCAN
rs3759115	C12orf65	cis	cerebellum	SCAN
rs3759115	CDK2AP1	Cis_1M	lymphoblastoid	RTeQTL
rs3759115	CDK2AP1	cis	cerebellum	SCAN
rs3759115	PITPNM2	cis	cerebellum	SCAN
rs3759115	MPHOSPH9	Cis_1M	lymphoblastoid	RTeQTL
rs3759115	RP11-282O18.3	cis	Esophagus Mucosa	GTEx
rs3759115	CDK2AP1	cis	Esophagus Mucosa	GTEx
rs3759115	ARL6IP4	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:123460600-123464600	Weak transcription	Aorta	Aorta
2	chr12:123460800-123464600	Genic enhancers	Spleen	Spleen
3	chr12:123461000-123464400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr12:123461000-123464400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr12:123461400-123473200	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr12:123463000-123464600	Enhancers	Liver	Liver
7	chr12:123463400-123464400	Enhancers	HMEC	breast
8	chr12:123463400-123464600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
9	chr12:123463600-123464400	Enhancers	Primary monocytes fromperipheralblood	blood
10	chr12:123463600-123464400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
11	chr12:123463600-123464400	Transcr. at gene 5' and 3'	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr12:123463600-123464400	Enhancers	Fetal Brain Male	brain
13	chr12:123463600-123464400	Enhancers	Lung	lung
14	chr12:123463600-123464400	Enhancers	Placenta Amnion	Placenta Amnion
15	chr12:123463600-123464600	Enhancers	Left Ventricle	heart
16	chr12:123463600-123464800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr12:123463600-123465000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr12:123463600-123465000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr12:123463800-123464400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr12:123463800-123464400	Enhancers	Primary T helper naive cells from peripheral blood	blood
21	chr12:123463800-123464400	Transcr. at gene 5' and 3'	Fetal Intestine Small	intestine
22	chr12:123463800-123464400	Enhancers	Gastric	stomach
23	chr12:123463800-123464400	Enhancers	Right Ventricle	heart
24	chr12:123463800-123464400	Weak transcription	Sigmoid Colon	Sigmoid Colon
25	chr12:123463800-123464600	Flanking Active TSS	Fetal Intestine Large	intestine
26	chr12:123463800-123464600	Enhancers	Small Intestine	intestine
27	chr12:123463800-123464600	Flanking Active TSS	Osteobl	bone
28	chr12:123463800-123464800	Flanking Active TSS	Duodenum Mucosa	Duodenum
29	chr12:123463800-123464800	Flanking Active TSS	HSMM	muscle
30	chr12:123463800-123464800	Flanking Active TSS	NH-A	brain
31	chr12:123463800-123465000	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
32	chr12:123463800-123465000	Flanking Active TSS	Brain Germinal Matrix	brain
33	chr12:123463800-123465000	Flanking Active TSS	Pancreas	Pancrea
34	chr12:123463800-123465000	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
35	chr12:123463800-123465000	Flanking Active TSS	Stomach Smooth Muscle	stomach
36	chr12:123463800-123466400	Active TSS	ES-I3 Cell Line	embryonic stem cell
37	chr12:123464000-123464400	Transcr. at gene 5' and 3'	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr12:123464000-123464400	Enhancers	Primary neutrophils fromperipheralblood	blood
39	chr12:123464000-123464400	Transcr. at gene 5' and 3'	Primary hematopoietic stem cells short term culture	blood
40	chr12:123464000-123464400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
41	chr12:123464000-123464400	Enhancers	Brain Anterior Caudate	brain
42	chr12:123464000-123464400	Enhancers	Esophagus	oesophagus
43	chr12:123464000-123464400	Transcr. at gene 5' and 3'	Fetal Adrenal Gland	Adrenal Gland
44	chr12:123464000-123464400	Enhancers	Fetal Heart	heart
45	chr12:123464000-123464400	Enhancers	Psoas Muscle	Psoas
46	chr12:123464000-123464600	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr12:123464000-123464600	Flanking Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr12:123464000-123464600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr12:123464000-123464600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr12:123464000-123464600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin

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