Variant report

Variant	rs35015427
Chromosome Location	chr12:9800639-9800640
allele	C/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	STAT1	chr12:9800284-9801263	GM12878	blood:	n/a	chr12:9800489-9800496 chr12:9800768-9800780
2	IRF3	chr12:9800634-9800691	GM12878	blood:	n/a	n/a
3	GABPA	chr12:9800275-9801002	A549	lung:	n/a	n/a
4	MXI1	chr12:9800287-9802771	GM12878	blood:	n/a	n/a
5	GABPA	chr12:9800034-9801209	A549	lung:	n/a	n/a
6	GABPA	chr12:9800316-9801165	HL-60	blood:	n/a	n/a
7	UBTF	chr12:9800050-9801395	K562	blood:	n/a	n/a
8	STAT3	chr12:9800517-9800681	MCF10A-Er-Src	breast:	n/a	n/a
9	MYC	chr12:9800560-9801184	MCF10A-Er-Src	breast:	n/a	n/a
10	BRCA1	chr12:9800286-9801460	Hela-S3	cervix:	n/a	n/a
11	CHD1	chr12:9800337-9804156	GM12878	blood:	n/a	chr12:9800667-9800677 chr12:9800660-9800670
12	TBL1XR1	chr12:9799984-9802966	GM12878	blood:	n/a	n/a
13	POLR2A	chr12:9799451-9804403	GM19193	blood:	n/a	n/a
14	MAX	chr12:9800424-9801178	A549	lung:	n/a	n/a
15	TAF1	chr12:9800589-9801123	GM12892	blood:	n/a	n/a
16	EP300	chr12:9800236-9801592	ECC-1	luminal epithelium:	n/a	chr12:9800672-9800688 chr12:9800673-9800689
17	RUNX3	chr12:9799672-9801651	GM12878	blood:	n/a	chr12:9800805-9800822
18	POLR2A	chr12:9800283-9801270	Hela-S3	cervix:	n/a	n/a
19	MTA3	chr12:9799406-9804477	GM12878	blood:	n/a	n/a
20	JUND	chr12:9800476-9800993	H1-hESC	embryonic stem cell:	n/a	chr12:9800672-9800681
21	MAX	chr12:9800358-9801415	SK-N-SH	brain:	n/a	n/a
22	YY1	chr12:9800447-9801045	K562	blood:	n/a	chr12:9800569-9800580 chr12:9800565-9800579 chr12:9800682-9800693
23	TCF12	chr12:9800411-9801239	GM12878	blood:	n/a	n/a
24	POLR2A	chr12:9800240-9801076	SK-N-MC	brain:	n/a	n/a
25	EP300	chr12:9800363-9802584	GM12878	blood:	n/a	chr12:9801950-9801964 chr12:9802375-9802389 chr12:9800672-9800688 chr12:9800673-9800689
26	GABPA	chr12:9800347-9800878	HepG2	liver:	n/a	n/a
27	JUND	chr12:9800471-9800990	A549	lung:	n/a	chr12:9800672-9800681
28	SIN3AK20	chr12:9800384-9801007	SK-N-SH	brain:	n/a	n/a
29	EP300	chr12:9800520-9802522	GM12878	blood:	n/a	chr12:9801950-9801964 chr12:9802375-9802389 chr12:9800672-9800688 chr12:9800673-9800689
30	TBP	chr12:9800325-9800942	HepG2	liver:	n/a	n/a
31	POLR2A	chr12:9800075-9801532	U87	brain:	n/a	n/a
32	RUNX3	chr12:9799645-9802568	GM12878	blood:	n/a	chr12:9800805-9800822
33	POLR2A	chr12:9800372-9800924	H1-hESC	embryonic stem cell:	n/a	n/a
34	BHLHE40	chr12:9800302-9801534	K562	blood:	n/a	chr12:9800672-9800688 chr12:9800678-9800694
35	POLR2A	chr12:9800194-9801236	HepG2	liver:	n/a	n/a
36	MYC	chr12:9800404-9801328	K562	blood:	n/a	n/a
37	EGR1	chr12:9800345-9800872	ECC-1	luminal epithelium:	n/a	chr12:9800625-9800635 chr12:9800624-9800638 chr12:9800776-9800786 chr12:9800623-9800637
38	POLR2A	chr12:9799501-9804451	GM12891	blood:	n/a	n/a
39	IRF1	chr12:9799891-9802485	K562	blood:	n/a	chr12:9801699-9801712 chr12:9802381-9802392 chr12:9801697-9801711 chr12:9802380-9802394 chr12:9800630-9800644 chr12:9801698-9801711 chr12:9801737-9801744 chr12:9801701-9801712 chr12:9801702-9801712 chr12:9801699-9801713 chr12:9801700-9801714 chr12:9801698-9801712 chr12:9801699-9801713
40	MYC	chr12:9800589-9800917	HepG2	liver:	n/a	n/a
41	KAP1	chr12:9799906-9802085	U2OS	brain:	n/a	chr12:9800521-9800529
42	CTBP2	chr12:9800343-9801323	H1-hESC	embryonic stem cell:	n/a	n/a
43	PAX5	chr12:9800590-9801177	GM12891	blood:	n/a	chr12:9800961-9800980
44	GTF2F1	chr12:9800341-9800946	H1-hESC	embryonic stem cell:	n/a	n/a
45	POLR2A	chr12:9800322-9800958	A549	lung:	n/a	n/a
46	POLR2A	chr12:9799408-9804409	GM19099	blood:	n/a	n/a
47	EGR1	chr12:9800450-9800851	K562	blood:	n/a	chr12:9800625-9800635 chr12:9800624-9800638 chr12:9800776-9800786 chr12:9800623-9800637
48	E2F6	chr12:9800406-9800929	K562	blood:	n/a	chr12:9800667-9800678 chr12:9800668-9800680 chr12:9800566-9800576 chr12:9800777-9800792
49	EGR1	chr12:9800402-9800795	GM12878	blood:	n/a	chr12:9800625-9800635 chr12:9800624-9800638 chr12:9800776-9800786 chr12:9800623-9800637
50	HDAC2	chr12:9800395-9800793	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:9800619-9800669	IMR90	lung:	fetal
2	chr12:9800619-9800669	NB4	blood:	n/a
3	chr12:9800619-9800669	HEEpiC	esophagus:	n/a
4	chr12:9800619-9800669	ECC-1	luminal epithelium:	n/a
5	chr12:9800619-9800669	AG09319	gingival:	n/a
6	chr12:9800619-9800669	HNPCEpiC	eye:	n/a
7	chr12:9800619-9800669	SK-N-MC	brain:	n/a
8	chr12:9800619-9800669	GM12878	blood:	n/a
9	chr12:9800619-9800669	A549	lung:	n/a
10	chr12:9800619-9800669	AG04450	lung:	fetal
11	chr12:9800619-9800669	PANC-1	pancreas:	n/a
12	chr12:9800619-9800669	ProgFib	skin:	n/a
13	chr12:9800619-9800669	AG04449	skin:	fetal
14	chr12:9800619-9800669	AG09309	skin:	n/a
15	chr12:9800619-9800669	HCF	heart:	n/a
16	chr12:9800619-9800669	HCT-116	colon:	n/a
17	chr12:9800619-9800669	HepG2	liver:	n/a
18	chr12:9800619-9800669	HCPEpiC	choroid plexus:	n/a
19	chr12:9800619-9800669	BJ	skin:	n/a
20	chr12:9800619-9800669	HL-60	blood:	n/a
21	chr12:9800619-9800669	H1-hESC	embryonic stem cell:	embryo
22	chr12:9800619-9800669	SKMC	muscle:	n/a
23	chr12:9800619-9800669	RPTEC	kidney:	n/a
24	chr12:9800619-9800669	AoSMC	blood vessel:	n/a
25	chr12:9800619-9800669	HMEC	breast:	n/a
26	chr12:9800619-9800669	HUVEC	blood vessel:	n/a
27	chr12:9800619-9800669	HRE	kidney:	n/a
28	chr12:9800619-9800669	NHBE	bronchial:	n/a
29	chr12:9800619-9800669	HIPEpiC	eye:	n/a
30	chr12:9800619-9800669	Hela-S3	cervix:	n/a
31	chr12:9800619-9800669	GM06990	blood:	n/a
32	chr12:9800619-9800669	Jurkat	blood:	n/a
33	chr12:9800619-9800669	NH-A	brain:	n/a
34	chr12:9800619-9800669	MCF-7	breast:	n/a
35	chr12:9800619-9800669	HRPEpiC	eye:	n/a
36	chr12:9800619-9800669	T-47D	breast:	n/a
37	chr12:9800619-9800669	SK-N-SH_RA	brain:	n/a
38	chr12:9800619-9800669	LNCaP	prostate:	n/a
39	chr12:9800619-9800669	NT2-D1	testis:	n/a
40	chr12:9800619-9800669	CMK	blood:	n/a
41	chr12:9800619-9800669	PFSK-1	brain:	n/a
42	chr12:9800619-9800669	ovcar-3	ovarian:	n/a
43	chr12:9800619-9800669	GM12892	blood:	n/a
44	chr12:9800619-9800669	HEK293	kidney:	embryo
45	chr12:9800619-9800669	NHDF-neo	bronchial:	n/a
46	chr12:9800619-9800669	HPAEpiC	pulmonary alveolar:	n/a
47	chr12:9800619-9800669	BE2_C	brain:	n/a
48	chr12:9800619-9800669	U87	brain:	n/a
49	chr12:9800619-9800669	GM12891	blood:	n/a
50	chr12:9800619-9800669	K562	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:9799292..9802850-chr12:9823422..9827161,3	MCF-7	breast:
2	chr12:9799323..9802837-chr12:9803671..9808302,9	K562	blood:
3	chr12:9786143..9793024-chr12:9797652..9803573,13	MCF-7	breast:
4	chr12:9799537..9802341-chr12:9814175..9817797,3	K562	blood:
5	chr12:9798786..9803516-chr12:9803864..9807970,10	MCF-7	breast:
6	chr12:9785588..9787603-chr12:9798282..9800898,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000256442	TF binding region
ENSG00000256594	TF binding region
ENSG00000256442	CpG island
ENSG00000256594	CpG island
ENSG00000256594	Chromatin interaction
ENSG00000069493	Chromatin interaction

Extended variants
information (count: 82 )
Associated
traits (count: 6 )

rSNPs within LD-proxies of this variant (count:74)

rs_ID	r²[population]
rs10466762	1.00[ASN][1000 genomes]
rs10772005	1.00[ASN][1000 genomes]
rs10772006	1.00[ASN][1000 genomes]
rs10844236	0.89[AFR][1000 genomes];0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10844267	0.89[AFR][1000 genomes];0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10844327	1.00[ASN][1000 genomes]
rs10844350	1.00[ASN][1000 genomes]
rs10844351	1.00[ASN][1000 genomes]
rs10844352	1.00[ASN][1000 genomes]
rs10844353	1.00[ASN][1000 genomes]
rs10844359	1.00[ASN][1000 genomes]
rs10844369	0.89[ASN][1000 genomes]
rs11052207	0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11052209	0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11052234	0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11052235	1.00[ASN][1000 genomes]
rs11052245	1.00[ASN][1000 genomes]
rs11052254	0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11052282	0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs11608817	0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12310789	1.00[ASN][1000 genomes]
rs12366653	0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12366792	0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12809846	0.89[AFR][1000 genomes];0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12820641	0.89[AFR][1000 genomes];0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12830419	0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12831287	0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1560008	1.00[ASN][1000 genomes]
rs16913477	1.00[ASN][1000 genomes]
rs1863871	1.00[ASN][1000 genomes]
rs2114869	1.00[ASN][1000 genomes]
rs2162657	1.00[ASN][1000 genomes]
rs34323946	0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs34833649	0.89[AFR][1000 genomes];0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34981673	0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs35098654	0.89[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35181877	0.89[ASN][1000 genomes]
rs35280686	1.00[ASN][1000 genomes]
rs35561167	0.89[AFR][1000 genomes];0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35642909	0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs35671537	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs35884213	0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs55873283	1.00[ASN][1000 genomes]
rs61916061	0.89[AFR][1000 genomes];0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6488065	0.89[ASN][1000 genomes]
rs7132037	1.00[ASN][1000 genomes]
rs7136821	0.89[AFR][1000 genomes];0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7299738	1.00[ASN][1000 genomes]
rs7302110	0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7302746	1.00[ASN][1000 genomes]
rs7303246	0.89[ASN][1000 genomes]
rs7304321	1.00[ASN][1000 genomes]
rs7304464	1.00[ASN][1000 genomes]
rs7305937	1.00[ASN][1000 genomes]
rs7309800	1.00[ASN][1000 genomes]
rs7310405	1.00[ASN][1000 genomes]
rs7310516	1.00[ASN][1000 genomes]
rs7310568	1.00[ASN][1000 genomes]
rs7310790	1.00[ASN][1000 genomes]
rs7311421	1.00[ASN][1000 genomes]
rs7311574	1.00[ASN][1000 genomes]
rs7311945	1.00[ASN][1000 genomes]
rs7959406	1.00[ASN][1000 genomes]
rs7959726	1.00[ASN][1000 genomes]
rs7961262	0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7961416	0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7962321	1.00[ASN][1000 genomes]
rs7967102	0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7973603	1.00[ASN][1000 genomes]
rs7974871	1.00[ASN][1000 genomes]
rs7978187	1.00[ASN][1000 genomes]
rs958340	1.00[ASN][1000 genomes]
rs9919786	1.00[ASN][1000 genomes]
rs9919787	0.89[ASN][1000 genomes]

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	nsv427903	chr12:9371593-9830668	Active TSS Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	34 gene(s)	inside rSNPs	diseases
2	esv2758293	chr12:9371595-9923529	Weak transcription Enhancers Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	40 gene(s)	inside rSNPs	diseases
3	esv2759878	chr12:9371595-9923529	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	40 gene(s)	inside rSNPs	diseases
4	esv1821732	chr12:9560087-9830668	Strong transcription Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
5	esv1823760	chr12:9560087-9830668	Weak transcription Active TSS ZNF genes & repeats Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
6	nsv428271	chr12:9560087-9830668	Enhancers Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
7	esv2757489	chr12:9583455-9810764	Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
8	nsv917178	chr12:9637315-9820153	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases

mRNA abundance (count:6)

SNP	Gene	Cis/trans	Tissue	Source
rs35015427	RP11-705C15.3	cis	Skin Sun Exposed Lower leg	GTEx
rs35015427	CLEC2D	cis	Esophagus Muscularis	GTEx
rs35015427	LOC728715,OVOS,LOC100134040,OVOS2	cis	brain	BrainEAC
rs35015427	RP11-705C15.3	cis	Whole Blood	GTEx
rs35015427	LOC374443	Cis_1M	lymphoblastoid	RTeQTL
rs35015427	CLEC2D	cis	Thyroid	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:9799800-9800800	Flanking Active TSS	Primary B cells from cord blood	blood
2	chr12:9799800-9800800	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
3	chr12:9799800-9801400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr12:9799800-9801800	Active TSS	HUES48 Cell Line	embryonic stem cell
5	chr12:9799800-9802200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
6	chr12:9799800-9803600	Flanking Active TSS	Primary hematopoietic stem cells	blood
7	chr12:9800000-9801000	Active TSS	Fetal Brain Female	brain
8	chr12:9800000-9801200	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr12:9800000-9801800	Active TSS	H1 Cell Line	embryonic stem cell
10	chr12:9800000-9801800	Active TSS	Duodenum Smooth Muscle	Duodenum
11	chr12:9800000-9802000	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr12:9800000-9802000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr12:9800000-9802000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
14	chr12:9800000-9802200	Active TSS	Brain Germinal Matrix	brain
15	chr12:9800000-9802800	Active TSS	ES-I3 Cell Line	embryonic stem cell
16	chr12:9800000-9802800	Active TSS	Fetal Kidney	kidney
17	chr12:9800000-9803400	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
18	chr12:9800000-9803600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr12:9800000-9804000	Active TSS	Rectal Smooth Muscle	rectum
20	chr12:9800200-9801000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr12:9800200-9801200	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr12:9800200-9801200	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
23	chr12:9800200-9801200	Flanking Active TSS	Dnd41	blood
24	chr12:9800200-9801400	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr12:9800200-9801400	Flanking Active TSS	Liver	Liver
26	chr12:9800200-9801600	Active TSS	Gastric	stomach
27	chr12:9800200-9801800	Active TSS	H9 Cell Line	embryonic stem cell
28	chr12:9800200-9801800	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr12:9800200-9801800	Active TSS	A549	lung
30	chr12:9800200-9802000	Active TSS	Brain Inferior Temporal Lobe	brain
31	chr12:9800200-9802000	Active TSS	Fetal Intestine Small	intestine
32	chr12:9800200-9802000	Active TSS	Left Ventricle	heart
33	chr12:9800200-9802000	Active TSS	Psoas Muscle	Psoas
34	chr12:9800200-9802200	Active TSS	Aorta	Aorta
35	chr12:9800200-9802200	Active TSS	Brain Cingulate Gyrus	brain
36	chr12:9800200-9802200	Flanking Active TSS	HMEC	breast
37	chr12:9800200-9802400	Active TSS	iPS-15b Cell Line	embryonic stem cell
38	chr12:9800200-9802400	Active TSS	Pancreatic Islets	Pancreatic Islet
39	chr12:9800200-9802400	Flanking Active TSS	HUVEC	blood vessel
40	chr12:9800200-9802600	Active TSS	HUES64 Cell Line	embryonic stem cell
41	chr12:9800200-9802600	Active TSS	Colon Smooth Muscle	Colon
42	chr12:9800200-9802600	Active TSS	Ovary	ovary
43	chr12:9800200-9802800	Active TSS	NHDF-Ad	bronchial
44	chr12:9800200-9803400	Active TSS	Brain Anterior Caudate	brain
45	chr12:9800200-9803400	Active TSS	Esophagus	oesophagus
46	chr12:9800200-9803400	Active TSS	Right Ventricle	heart
47	chr12:9800200-9803400	Active TSS	HSMMtube	muscle
48	chr12:9800200-9803600	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
49	chr12:9800200-9804000	Active TSS	Right Atrium	heart
50	chr12:9800400-9800800	Transcr. at gene 5' and 3'	iPS DF 19.11 Cell Line	embryonic stem cell

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