Variant report

Variant	rs1790106
Chromosome Location	chr12:123591596-123591597
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:50)
CpG islands
(count:0)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	JUND	chr12:123591474-123591865	K562	blood:	n/a	n/a
2	NFIC	chr12:123591439-123592002	ECC-1	luminal epithelium:	n/a	chr12:123591918-123591935
3	MAX	chr12:123591449-123591956	K562	blood:	n/a	n/a
4	GABPA	chr12:123591559-123591898	K562	blood:	n/a	n/a
5	RCOR1	chr12:123591429-123591905	Hela-S3	cervix:	n/a	n/a
6	MAZ	chr12:123591518-123591963	K562	blood:	n/a	n/a
7	GABPA	chr12:123591345-123592018	K562	blood:	n/a	n/a
8	ELF1	chr12:123591574-123591981	GM12878	blood:	n/a	chr12:123591729-123591742
9	TCF12	chr12:123591248-123592186	ECC-1	luminal epithelium:	n/a	n/a
10	TBP	chr12:123591559-123591992	Hela-S3	cervix:	n/a	n/a
11	POLR2A	chr12:123591361-123592150	Hela-S3	cervix:	n/a	n/a
12	TFAP2C	chr12:123591122-123591961	Hela-S3	cervix:	n/a	chr12:123591309-123591324
13	RCOR1	chr12:123591382-123591853	K562	blood:	n/a	n/a
14	MAZ	chr12:123591409-123591995	Hela-S3	cervix:	n/a	n/a
15	POLR2A	chr12:123591562-123591909	GM12878	blood:	n/a	n/a
16	SMC3	chr12:123591468-123591984	Hela-S3	cervix:	n/a	n/a
17	ELF1	chr12:123591564-123591940	K562	blood:	n/a	chr12:123591729-123591742
18	EP300	chr12:123591264-123592195	ECC-1	luminal epithelium:	n/a	chr12:123591635-123591642
19	ZBTB7A	chr12:123591534-123592028	K562	blood:	n/a	n/a
20	TCF12	chr12:123591380-123592075	ECC-1	luminal epithelium:	n/a	n/a
21	USF2	chr12:123591594-123591794	Hela-S3	cervix:	n/a	n/a
22	GABPA	chr12:123591595-123591963	Hela-S3	cervix:	n/a	n/a
23	EP300	chr12:123591355-123592111	ECC-1	luminal epithelium:	n/a	chr12:123591635-123591642
24	BHLHE40	chr12:123591532-123591757	K562	blood:	n/a	n/a
25	JUN	chr12:123591045-123591941	K562	blood:	n/a	n/a
26	POLR2A	chr12:123591457-123592047	Hela-S3	cervix:	n/a	n/a
27	RUNX3	chr12:123591490-123591815	GM12878	blood:	n/a	n/a
28	MAX	chr12:123591167-123592438	NB4	blood:	n/a	n/a
29	HCFC1	chr12:123590882-123592180	Hela-S3	cervix:	n/a	n/a
30	NR2F2	chr12:123591494-123591845	K562	blood:	n/a	n/a
31	NR2F2	chr12:123591438-123591957	K562	blood:	n/a	n/a
32	ELK4	chr12:123591573-123592009	Hela-S3	cervix:	n/a	chr12:123591732-123591743
33	MYC	chr12:123591211-123592300	NB4	blood:	n/a	n/a
34	POLR2A	chr12:123591577-123591914	GM12878	blood:	n/a	n/a
35	CBX3	chr12:123591481-123591946	K562	blood:	n/a	n/a
36	ELF1	chr12:123591173-123592079	GM12878	blood:	n/a	chr12:123591729-123591742
37	MYC	chr12:123591490-123591927	K562	blood:	n/a	n/a
38	STAT3	chr12:123591569-123591835	Hela-S3	cervix:	n/a	n/a
39	MAZ	chr12:123591449-123591894	GM12878	blood:	n/a	n/a
40	MAX	chr12:123591585-123591817	K562	blood:	n/a	n/a
41	RAD21	chr12:123591464-123591673	K562	blood:	n/a	n/a
42	CHD2	chr12:123591502-123591937	Hela-S3	cervix:	n/a	n/a
43	ELF1	chr12:123591482-123591961	K562	blood:	n/a	chr12:123591729-123591742
44	POLR2A	chr12:123591295-123592051	NB4	blood:	n/a	n/a
45	RAD21	chr12:123591388-123591962	Hela-S3	cervix:	n/a	n/a
46	GTF2F1	chr12:123591372-123592150	Hela-S3	cervix:	n/a	n/a
47	MAX	chr12:123591338-123592025	Hela-S3	cervix:	n/a	n/a
48	POLR2A	chr12:123591545-123592010	Hela-S3	cervix:	n/a	n/a
49	ELK1	chr12:123591561-123591962	Hela-S3	cervix:	n/a	n/a
50	POLR2A	chr12:123591419-123591984	HL-60	blood:	n/a	n/a

No data

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:123591372..123592151-chr15:41624410..41625118,2	NB4	blood:
2	chr12:123579230..123579753-chr12:123591042..123591628,2	MCF-7	breast:
3	chr12:123553960..123555142-chr12:123590854..123591747,7	MCF-7	breast:
4	chr12:123554110..123555021-chr12:123590854..123591747,3	MCF-7	breast:
5	chr12:123500117..123502770-chr12:123590126..123592827,2	K562	blood:
6	chr12:123587888..123589723-chr12:123591389..123594363,2	MCF-7	breast:

No data

Variant related genes	Relation type
PITPNM2	TF binding region
ENSG00000137804	Chromatin interaction
ENSG00000104147	Chromatin interaction
ENSG00000265603	Chromatin interaction

Extended variants
information (count: 68 )
Associated
traits (count: 10 )

rSNPs within LD-proxies of this variant (count:62)

rs_ID	r²[population]
rs1051434	0.96[CEU][hapmap];0.82[CHB][hapmap];0.82[CHD][hapmap];0.90[GIH][hapmap];0.80[JPT][hapmap];0.95[MEX][hapmap];0.97[TSI][hapmap];1.00[YRI][hapmap];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10773002	0.83[ASW][hapmap]
rs10773003	0.80[JPT][hapmap]
rs10773005	0.80[JPT][hapmap]
rs10773921	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];0.86[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10846489	1.00[ASW][hapmap];0.84[CEU][hapmap];1.00[LWK][hapmap];0.88[MEX][hapmap];0.84[MKK][hapmap];0.83[TSI][hapmap];1.00[YRI][hapmap]
rs10848428	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];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11057251	0.90[ASW][hapmap];0.80[JPT][hapmap];0.90[LWK][hapmap];0.83[MEX][hapmap];0.84[MKK][hapmap];1.00[YRI][hapmap]
rs11060853	0.81[JPT][hapmap]
rs1109559	1.00[ASW][hapmap];0.80[CEU][hapmap];1.00[LWK][hapmap];0.91[MEX][hapmap];0.84[MKK][hapmap];1.00[YRI][hapmap]
rs11608305	0.80[JPT][hapmap]
rs11608811	0.90[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[GIH][hapmap];0.90[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11610710	0.89[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs11613937	0.85[AFR][1000 genomes];0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12229700	0.89[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12317452	0.80[JPT][hapmap]
rs12425009	0.90[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];0.86[GIH][hapmap];0.86[JPT][hapmap];0.84[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.82[EUR][1000 genomes]
rs12425850	1.00[YRI][hapmap];0.82[EUR][1000 genomes]
rs1568427	0.83[ASW][hapmap]
rs1568428	1.00[ASW][hapmap];0.84[CEU][hapmap];1.00[LWK][hapmap];0.88[MEX][hapmap];0.84[MKK][hapmap];0.80[TSI][hapmap];1.00[YRI][hapmap]
rs1611973	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1615350	0.83[ASW][hapmap];0.83[CHB][hapmap];0.82[CHD][hapmap];0.85[JPT][hapmap];0.82[TSI][hapmap]
rs1626703	0.84[AFR][1000 genomes]
rs1716178	0.82[AMR][1000 genomes]
rs1716184	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1727286	0.90[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs1727293	1.00[ASW][hapmap];0.96[CEU][hapmap];0.91[CHB][hapmap];0.82[CHD][hapmap];0.90[GIH][hapmap];0.90[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];0.97[TSI][hapmap];1.00[YRI][hapmap];0.92[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1727295	0.91[CEU][hapmap];0.95[CHB][hapmap];0.83[JPT][hapmap];1.00[YRI][hapmap];0.97[AMR][1000 genomes];0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1727301	0.85[JPT][hapmap]
rs1727302	0.83[CHB][hapmap];0.82[CHD][hapmap];0.85[JPT][hapmap];0.82[TSI][hapmap]
rs1727305	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1727307	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1727312	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1790088	0.89[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs1790094	0.90[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];0.95[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1790096	0.84[AFR][1000 genomes]
rs1790104	0.85[JPT][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes]
rs1790121	0.90[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.91[LWK][hapmap];1.00[MEX][hapmap];0.91[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1790122	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1790129	0.90[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs1790134	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs1879379	1.00[ASW][hapmap];0.91[LWK][hapmap];0.91[MEX][hapmap];0.84[MKK][hapmap];1.00[YRI][hapmap]
rs1984658	0.81[EUR][1000 genomes]
rs2682427	0.85[JPT][hapmap]
rs28755851	0.80[EUR][1000 genomes]
rs3088303	0.80[JPT][hapmap]
rs3741530	1.00[CEU][hapmap];0.80[EUR][1000 genomes]
rs3759115	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]
rs3897102	1.00[CHB][hapmap];0.81[JPT][hapmap]
rs4148862	0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4148863	0.90[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];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4275659	1.00[ASW][hapmap];1.00[CEU][hapmap];0.95[CHB][hapmap];0.83[GIH][hapmap];0.86[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.91[MKK][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap]
rs585522	0.80[GIH][hapmap]
rs7135296	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];0.82[GIH][hapmap];0.85[JPT][hapmap];1.00[LWK][hapmap];0.96[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.81[EUR][1000 genomes]
rs7139321	1.00[YRI][hapmap];0.82[AFR][1000 genomes]
rs7296418	0.91[CEU][hapmap];0.95[CHB][hapmap];0.82[GIH][hapmap];0.86[JPT][hapmap];0.97[TSI][hapmap]
rs7304782	0.83[ASW][hapmap]
rs7305511	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];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.81[EUR][1000 genomes]
rs7957096	1.00[CEU][hapmap];0.91[CHB][hapmap];0.90[JPT][hapmap];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs884956	1.00[ASW][hapmap];0.95[CHB][hapmap];0.90[LWK][hapmap];0.91[MEX][hapmap];0.95[MKK][hapmap];1.00[YRI][hapmap]
rs940904	0.80[GIH][hapmap]
rs949143	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];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 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	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
3	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
4	nsv1042550	chr12:123532028-123659500	Flanking Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Bivalent Enhancer ZNF genes & repeats 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	18 gene(s)	inside rSNPs	diseases
5	esv1825473	chr12:123582855-123822503	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
6	nsv870326	chr12:123585990-123719323	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases

mRNA abundance (count:10)

SNP	Gene	Cis/trans	Tissue	Source
rs1790106	RP11-282O18.3	cis	Esophagus Mucosa	GTEx
rs1790106	MPHOSPH9	Cis_1M	lymphoblastoid	RTeQTL
rs1790106	PITPNM2	cis	cerebellum	SCAN
rs1790106	CDK2AP1	Cis_1M	lymphoblastoid	RTeQTL
rs1790106	CDK2AP1	cis	cerebellum	SCAN
rs1790106	SBNO1	Cis_1M	lymphoblastoid	RTeQTL
rs1790106	ARL6IP4	Cis_1M	lymphoblastoid	RTeQTL
rs1790106	CDK2AP1	cis	Esophagus Mucosa	GTEx
rs1790106	TMEM120B	cis	parietal	SCAN
rs1790106	C12orf65	cis	cerebellum	SCAN

Chromatin state (count:118 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:123561600-123604000	Genic enhancers	Fetal Thymus	thymus
2	chr12:123571200-123600000	Genic enhancers	Thymus	Thymus
3	chr12:123579800-123593600	Weak transcription	Fetal Intestine Large	intestine
4	chr12:123579800-123596200	Weak transcription	Osteobl	bone
5	chr12:123580000-123592600	Weak transcription	NHEK	skin
6	chr12:123580000-123593800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr12:123580200-123593200	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr12:123580600-123596000	Weak transcription	Placenta Amnion	Placenta Amnion
9	chr12:123581000-123593000	Weak transcription	Pancreas	Pancrea
10	chr12:123581200-123593000	Weak transcription	Brain Germinal Matrix	brain
11	chr12:123581400-123591600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr12:123582800-123592600	Weak transcription	Gastric	stomach
13	chr12:123583000-123595800	Weak transcription	NHDF-Ad	bronchial
14	chr12:123583200-123599600	Weak transcription	Pancreatic Islets	Pancreatic Islet
15	chr12:123583600-123591800	Weak transcription	HSMMtube	muscle
16	chr12:123583600-123592000	Weak transcription	Duodenum Smooth Muscle	Duodenum
17	chr12:123584600-123593400	Weak transcription	Colonic Mucosa	Colon
18	chr12:123584800-123591800	Weak transcription	Colon Smooth Muscle	Colon
19	chr12:123586000-123592600	Enhancers	iPS-15b Cell Line	embryonic stem cell
20	chr12:123586800-123592200	Enhancers	HepG2	liver
21	chr12:123587200-123591600	Enhancers	Primary T cells from cord blood	blood
22	chr12:123587200-123595600	Enhancers	Liver	Liver
23	chr12:123588000-123599000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr12:123588200-123592000	Weak transcription	NHLF	lung
25	chr12:123588200-123592800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr12:123588200-123593200	Weak transcription	Ovary	ovary
27	chr12:123589400-123592000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr12:123589400-123592000	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr12:123589400-123592200	Enhancers	H1 Cell Line	embryonic stem cell
30	chr12:123589400-123592200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr12:123589400-123592200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr12:123589400-123592800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
33	chr12:123589400-123593000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
34	chr12:123589400-123593000	Enhancers	Placenta	Placenta
35	chr12:123589400-123594200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
36	chr12:123589400-123595400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr12:123589600-123592200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr12:123589600-123593600	Enhancers	Primary monocytes fromperipheralblood	blood
39	chr12:123589600-123595200	Enhancers	Skeletal Muscle Female	skeletal muscle
40	chr12:123589800-123592200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr12:123590000-123592000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr12:123590000-123592400	Enhancers	HUVEC	blood vessel
43	chr12:123590000-123592600	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr12:123590000-123593800	Enhancers	Fetal Heart	heart
45	chr12:123590000-123595200	Strong transcription	Fetal Intestine Small	intestine
46	chr12:123590000-123596600	Enhancers	Right Ventricle	heart
47	chr12:123590000-123598200	Enhancers	Right Atrium	heart
48	chr12:123590000-123603800	Enhancers	Left Ventricle	heart
49	chr12:123590200-123592200	Genic enhancers	Brain Dorsolateral Prefrontal Cortex	brain
50	chr12:123590200-123592600	Enhancers	Primary B cells from peripheral blood	blood

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