Variant report

Variant	rs6755303
Chromosome Location	chr2:47169003-47169004
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:409)
CpG islands
(count:61)
Chromatin interactive
region (count:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:409 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	RAD21	chr2:47168551-47169370	A549	lung:	n/a	n/a
2	HEY1	chr2:47168610-47169265	HepG2	liver:	n/a	n/a
3	CTCF	chr2:47168880-47169030	HCPEpiC	choroid plexus:	n/a	chr2:47168914-47168927
4	RELA	chr2:47168667-47169932	GM19193	blood:	n/a	n/a
5	TAF1	chr2:47168660-47169118	Hela-S3	cervix:	n/a	n/a
6	CHD1	chr2:47168694-47169296	H1-hESC	embryonic stem cell:	n/a	n/a
7	E2F4	chr2:47167993-47169602	K562	blood:	n/a	chr2:47169461-47169468 chr2:47168901-47168909 chr2:47168899-47168910 chr2:47169461-47169468 chr2:47168108-47168120 chr2:47168958-47168968 chr2:47169457-47169469 chr2:47169461-47169468
8	POLR2A	chr2:47168048-47169610	GM12878	blood:	n/a	n/a
9	POLR2A	chr2:47168835-47169161	K562	blood:	n/a	n/a
10	POLR2A	chr2:47168038-47169209	K562	blood:	n/a	n/a
11	TCF3	chr2:47168108-47169060	GM12878	blood:	n/a	n/a
12	POLR2A	chr2:47168245-47169855	GM12892	blood:	n/a	n/a
13	MAX	chr2:47168564-47169187	SK-N-SH	brain:	n/a	chr2:47169037-47169048
14	CTCF	chr2:47168900-47169050	A549	lung:	n/a	chr2:47168914-47168927
15	TAF1	chr2:47168110-47169018	HepG2	liver:	n/a	n/a
16	TCF12	chr2:47168679-47169018	GM12878	blood:	n/a	n/a
17	CREB1	chr2:47167831-47169080	A549	lung:	n/a	chr2:47168009-47168022
18	TBP	chr2:47168783-47169900	GM12878	blood:	n/a	n/a
19	E2F6	chr2:47168563-47169108	K562	blood:	n/a	chr2:47168901-47168909 chr2:47168958-47168968
20	ZBTB7A	chr2:47167467-47169239	ECC-1	luminal epithelium:	n/a	n/a
21	CTCF	chr2:47168900-47169050	HUVEC	blood vessel:	n/a	chr2:47168914-47168927
22	STAT3	chr2:47168740-47169082	MCF10A-Er-Src	breast:	n/a	n/a
23	POLR2A	chr2:47167996-47169186	K562	blood:	n/a	n/a
24	CTCF	chr2:47168920-47169070	NB4	blood:	n/a	n/a
25	POLR2A	chr2:47167706-47169478	HUVEC	blood vessel:	n/a	n/a
26	YY1	chr2:47168081-47169510	GM12892	blood:	n/a	chr2:47168670-47168690 chr2:47168245-47168259 chr2:47168676-47168688
27	RCOR1	chr2:47168725-47169405	Hela-S3	cervix:	n/a	n/a
28	MAX	chr2:47167603-47169355	K562	blood:	n/a	chr2:47168106-47168116 chr2:47169037-47169048 chr2:47167751-47167760
29	CTCF	chr2:47168880-47169030	HCM	heart:	n/a	chr2:47168914-47168927
30	MAX	chr2:47168615-47169131	A549	lung:	n/a	chr2:47169037-47169048
31	ZNF143	chr2:47168853-47169103	K562	blood:	n/a	n/a
32	CTCF	chr2:47168860-47169010	HMEC	breast:	n/a	chr2:47168914-47168927
33	POLR2A	chr2:47167805-47169022	A549	lung:	n/a	n/a
34	RUNX3	chr2:47168562-47169995	GM12878	blood:	n/a	chr2:47169041-47169056
35	MYC	chr2:47167697-47169785	NB4	blood:	n/a	chr2:47168106-47168116 chr2:47169037-47169048 chr2:47167751-47167760
36	EP300	chr2:47168724-47169035	GM12878	blood:	n/a	chr2:47168948-47168964
37	CHD2	chr2:47168605-47169105	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr2:47168880-47169030	HCFaa	heart:	n/a	chr2:47168914-47168927
39	ELF1	chr2:47168697-47169137	K562	blood:	n/a	n/a
40	POLR2A	chr2:47168032-47169485	MCF-7	breast:	n/a	n/a
41	MXI1	chr2:47166976-47169461	HepG2	liver:	n/a	n/a
42	CTCF	chr2:47168880-47169030	HVMF	connective:	n/a	chr2:47168914-47168927
43	TEAD4	chr2:47168665-47169125	H1-hESC	embryonic stem cell:	n/a	n/a
44	GATA3	chr2:47167309-47169655	A549	lung:	n/a	chr2:47169431-47169439
45	CTCF	chr2:47168960-47169110	Hela-S3	cervix:	n/a	n/a
46	ELF1	chr2:47168711-47169094	HepG2	liver:	n/a	n/a
47	ELF1	chr2:47168142-47169118	GM12878	blood:	n/a	chr2:47168240-47168252
48	POLR2A	chr2:47168634-47169056	HepG2	liver:	n/a	n/a
49	CTCF	chr2:47168920-47169070	GM12873	blood:	n/a	n/a
50	CTCF	chr2:47168860-47169010	HepG2	liver:	n/a	chr2:47168914-47168927

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:47168977-47169027	AoSMC	blood vessel:	n/a
2	chr2:47168977-47169027	BJ	skin:	n/a
3	chr2:47168977-47169027	Hela-S3	cervix:	n/a
4	chr2:47168977-47169027	NHDF-neo	bronchial:	n/a
5	chr2:47168977-47169027	HCPEpiC	choroid plexus:	n/a
6	chr2:47168977-47169027	AG04450	lung:	fetal
7	chr2:47168977-47169027	HCF	heart:	n/a
8	chr2:47168977-47169027	AG04449	skin:	fetal
9	chr2:47168977-47169027	NH-A	brain:	n/a
10	chr2:47168977-47169027	AG10803	skin:	n/a
11	chr2:47168977-47169027	GM12878	blood:	n/a
12	chr2:47168977-47169027	GM19239	blood:	n/a
13	chr2:47168977-47169027	Hepatocyte	liver:	n/a
14	chr2:47168977-47169027	HEK293	kidney:	embryo
15	chr2:47168977-47169027	H1-hESC	embryonic stem cell:	embryo
16	chr2:47168977-47169027	SK-N-SH_RA	brain:	n/a
17	chr2:47168977-47169027	Caco-2	colon:	n/a
18	chr2:47168977-47169027	K562	blood:	n/a
19	chr2:47168977-47169027	HCT-116	colon:	n/a
20	chr2:47168977-47169027	ECC-1	luminal epithelium:	n/a
21	chr2:47168977-47169027	SK-N-SH	brain:	n/a
22	chr2:47168977-47169027	ovcar-3	ovarian:	n/a
23	chr2:47168977-47169027	PFSK-1	brain:	n/a
24	chr2:47168977-47169027	HRE	kidney:	n/a
25	chr2:47168977-47169027	HIPEpiC	eye:	n/a
26	chr2:47168977-47169027	HMEC	breast:	n/a
27	chr2:47168977-47169027	SAEC	small airway:	n/a
28	chr2:47168977-47169027	GM12891	blood:	n/a
29	chr2:47168977-47169027	SKMC	muscle:	n/a
30	chr2:47168977-47169027	HEEpiC	esophagus:	n/a
31	chr2:47168977-47169027	HRCEpiC	kidney:	n/a
32	chr2:47168977-47169027	HUVEC	blood vessel:	n/a
33	chr2:47168977-47169027	NT2-D1	testis:	n/a
34	chr2:47168977-47169027	ProgFib	skin:	n/a
35	chr2:47168977-47169027	NHBE	bronchial:	n/a
36	chr2:47168977-47169027	IMR90	lung:	fetal
37	chr2:47168977-47169027	RPTEC	kidney:	n/a
38	chr2:47168977-47169027	MCF10A-Er-Src	breast:	n/a
39	chr2:47168977-47169027	Jurkat	blood:	n/a
40	chr2:47168977-47169027	U87	brain:	n/a
41	chr2:47168977-47169027	NB4	blood:	n/a
42	chr2:47168977-47169027	HL-60	blood:	n/a
43	chr2:47168977-47169027	HepG2	liver:	n/a
44	chr2:47168977-47169027	HPAEpiC	pulmonary alveolar:	n/a
45	chr2:47168977-47169027	HAEpiC	amniotic membrane:	n/a
46	chr2:47168977-47169027	HRPEpiC	eye:	n/a
47	chr2:47168977-47169027	AG09309	skin:	n/a
48	chr2:47168977-47169027	MCF-7	breast:	n/a
49	chr2:47168977-47169027	LNCaP	prostate:	n/a
50	chr2:47168977-47169027	HCM	heart:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr2:47167461..47169104-chr2:47203278..47205346,2	MCF-7	breast:
2	chr2:47166915..47170495-chr2:47399445..47404516,7	MCF-7	breast:
3	chr2:47166485..47169114-chr2:47402596..47405123,4	MCF-7	breast:
4	chr2:47139463..47143529-chr2:47167839..47169953,4	K562	blood:
5	chr2:47135393..47141252-chr2:47166022..47170880,5	K562	blood:
6	chr2:47168040..47171171-chr2:47402063..47404163,4	K562	blood:
7	chr2:47165446..47170208-chr2:47173646..47177856,9	MCF-7	breast:
8	chr2:47143277..47146895-chr2:47166934..47170660,7	MCF-7	breast:
9	chr2:47167291..47170086-chr2:47204793..47207048,4	MCF-7	breast:
10	chr2:47139886..47146981-chr2:47165365..47170438,17	MCF-7	breast:
11	chr2:47168340..47172583-chr2:47183123..47189203,6	MCF-7	breast:
12	chr2:47141557..47143529-chr2:47167839..47169788,2	K562	blood:
13	chr2:47141053..47143152-chr2:47167792..47169429,2	MCF-7	breast:
14	chr2:47166107..47171055-chr2:47402078..47404965,9	K562	blood:

No data

Variant related genes	Relation type
MCFD2	TF binding region
MCFD2	CpG island
ENSG00000143933	Chromatin interaction
ENSG00000272814	Chromatin interaction
ENSG00000068724	Chromatin interaction
ENSG00000180398	Chromatin interaction

Extended variants
information (count: 72 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:65)

rs_ID	r²[population]
rs10174894	0.94[ASN][1000 genomes]
rs10199965	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs11890177	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs11894319	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs13388612	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap];0.98[ASN][1000 genomes]
rs13392448	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13398851	0.93[AFR][1000 genomes];0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs13423962	0.88[CEU][hapmap]
rs1446499	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs1446500	0.98[ASN][1000 genomes]
rs17035859	0.88[CHB][hapmap];0.89[JPT][hapmap];0.83[ASN][1000 genomes]
rs17035867	0.89[CHB][hapmap];0.91[JPT][hapmap];0.87[ASN][1000 genomes]
rs17035884	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs17035887	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs17036060	0.88[CHB][hapmap]
rs2084192	0.98[ASN][1000 genomes]
rs2289927	0.94[ASN][1000 genomes]
rs2289928	0.94[ASN][1000 genomes]
rs2347259	0.88[CHB][hapmap];0.89[JPT][hapmap];0.87[ASN][1000 genomes]
rs28516550	0.92[ASN][1000 genomes]
rs3087857	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs34581142	0.81[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs35433380	0.94[ASN][1000 genomes]
rs55872217	0.94[ASN][1000 genomes]
rs56213467	0.98[ASN][1000 genomes]
rs58589709	0.96[ASN][1000 genomes]
rs60194846	0.98[ASN][1000 genomes]
rs61132855	0.87[ASN][1000 genomes]
rs62136818	0.83[ASN][1000 genomes]
rs62136819	0.83[ASN][1000 genomes]
rs62136820	0.87[ASN][1000 genomes]
rs62136822	0.92[ASN][1000 genomes]
rs62136823	0.94[ASN][1000 genomes]
rs62136825	0.94[ASN][1000 genomes]
rs62136827	0.94[ASN][1000 genomes]
rs62140550	0.98[ASN][1000 genomes]
rs62140553	0.83[ASN][1000 genomes]
rs6544938	0.96[ASN][1000 genomes]
rs6544939	0.96[ASN][1000 genomes]
rs6706031	0.94[ASN][1000 genomes]
rs6715391	0.92[ASN][1000 genomes]
rs6715620	0.98[ASN][1000 genomes]
rs6716381	0.98[ASN][1000 genomes]
rs6722440	0.94[ASN][1000 genomes]
rs6729120	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs6729604	0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[YRI][hapmap];0.98[ASN][1000 genomes]
rs6733548	0.98[ASN][1000 genomes]
rs6743966	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs6743994	0.92[ASN][1000 genomes]
rs6745578	0.89[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs6758093	0.88[CEU][hapmap];1.00[CHB][hapmap];0.91[JPT][hapmap];0.87[YRI][hapmap];0.98[ASN][1000 genomes]
rs6758512	0.94[ASN][1000 genomes]
rs71423929	0.98[ASN][1000 genomes]
rs7340475	0.89[CHB][hapmap];0.91[JPT][hapmap];0.87[ASN][1000 genomes]
rs73926966	0.98[ASN][1000 genomes]
rs754411	0.89[CHB][hapmap];0.91[JPT][hapmap];0.87[ASN][1000 genomes]
rs7565420	0.89[ASN][1000 genomes]
rs7574514	0.89[CHB][hapmap];0.91[JPT][hapmap];0.83[ASN][1000 genomes]
rs7574833	0.88[CHB][hapmap];0.89[JPT][hapmap];0.81[ASN][1000 genomes]
rs7575172	0.98[ASN][1000 genomes]
rs7586004	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs7596198	0.92[ASN][1000 genomes]
rs7601491	0.98[ASN][1000 genomes]
rs8861	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs9973504	0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv817517	chr2:46819371-47715140	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Active TSS 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 miRNA miRNA target site	152 gene(s)	inside rSNPs	diseases
2	nsv457352	chr2:47004788-47325973	Active TSS Enhancers Genic enhancers Strong transcription Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
3	nsv581749	chr2:47004788-47325973	Flanking Active TSS Enhancers Genic enhancers Strong transcription Weak transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
4	nsv1004828	chr2:47056849-47814482	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	144 gene(s)	inside rSNPs	diseases
5	nsv524970	chr2:47162739-47302095	Enhancers Genic enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
6	esv3427405	chr2:47166973-47169821	Flanking Active TSS Bivalent/Poised TSS Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region	14 gene(s)	inside rSNPs	diseases
7	esv3332265	chr2:47167448-47169546	Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	14 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs6755303	MCFD2	cis	Adipose Subcutaneous	GTEx
rs6755303	MCFD2	cis	Artery Tibial	GTEx
rs6755303	MCFD2	cis	Muscle Skeletal	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:47167400-47169200	Active TSS	HUES48 Cell Line	embryonic stem cell
2	chr2:47167400-47169400	Transcr. at gene 5' and 3'	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr2:47167400-47169600	Active TSS	H9 Cell Line	embryonic stem cell
4	chr2:47167600-47169200	Active TSS	Brain Inferior Temporal Lobe	brain
5	chr2:47167600-47169200	Active TSS	Brain Substantia Nigra	brain
6	chr2:47167600-47169400	Active TSS	ES-I3 Cell Line	embryonic stem cell
7	chr2:47167600-47169400	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr2:47167600-47169600	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr2:47167600-47169600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr2:47167600-47169600	Active TSS	Primary T cells from cord blood	blood
11	chr2:47167600-47169600	Active TSS	Right Ventricle	heart
12	chr2:47167600-47169800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
13	chr2:47167600-47169800	Active TSS	Fetal Kidney	kidney
14	chr2:47167600-47169800	Active TSS	Pancreatic Islets	Pancreatic Islet
15	chr2:47167600-47170000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr2:47167600-47170400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr2:47167600-47170400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr2:47167600-47170400	Active TSS	Rectal Smooth Muscle	rectum
19	chr2:47167600-47170600	Active TSS	Thymus	Thymus
20	chr2:47167800-47169200	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr2:47167800-47169200	Active TSS	Primary B cells from peripheral blood	blood
22	chr2:47167800-47169200	Active TSS	Brain Angular Gyrus	brain
23	chr2:47167800-47169200	Active TSS	Brain Anterior Caudate	brain
24	chr2:47167800-47169200	Active TSS	Brain Cingulate Gyrus	brain
25	chr2:47167800-47169200	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
26	chr2:47167800-47169200	Active TSS	Colon Smooth Muscle	Colon
27	chr2:47167800-47169200	Active TSS	Rectal Mucosa Donor 31	rectum
28	chr2:47167800-47169400	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr2:47167800-47169400	Active TSS	iPS-15b Cell Line	embryonic stem cell
30	chr2:47167800-47169400	Active TSS	iPS-18 Cell Line	embryonic stem cell
31	chr2:47167800-47169400	Active TSS	Ovary	ovary
32	chr2:47167800-47169600	Active TSS	Primary monocytes fromperipheralblood	blood
33	chr2:47167800-47169600	Active TSS	Lung	lung
34	chr2:47167800-47169600	Active TSS	Hela-S3	cervix
35	chr2:47167800-47169800	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
36	chr2:47167800-47169800	Active TSS	Aorta	Aorta
37	chr2:47167800-47169800	Active TSS	Duodenum Smooth Muscle	Duodenum
38	chr2:47167800-47169800	Active TSS	Pancreas	Pancrea
39	chr2:47167800-47169800	Active TSS	Sigmoid Colon	Sigmoid Colon
40	chr2:47167800-47169800	Active TSS	A549	lung
41	chr2:47167800-47169800	Active TSS	Monocytes-CD14+_RO01746	blood
42	chr2:47167800-47170000	Active TSS	Esophagus	oesophagus
43	chr2:47167800-47170000	Active TSS	Spleen	Spleen
44	chr2:47167800-47170400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr2:47168000-47169200	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr2:47168000-47169200	Active TSS	Placenta	Placenta
47	chr2:47168000-47169200	Active TSS	NH-A	brain
48	chr2:47168000-47169200	Active TSS	NHEK	skin
49	chr2:47168000-47169400	Active TSS	Left Ventricle	heart
50	chr2:47168000-47169600	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived

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