Variant report

Variant	rs4141060
Chromosome Location	chr3:50300117-50300118
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:13)
CpG islands
(count:0)
Chromatin interactive
region (count:6)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:13 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr3:50300054-50300540	Hela-S3	cervix:	n/a	n/a
2	POLR2A	chr3:50299747-50300117	HepG2	liver:	n/a	n/a
3	POLR2A	chr3:50299915-50300684	K562	blood:	n/a	n/a
4	POLR2A	chr3:50299854-50300682	HepG2	liver:	n/a	n/a
5	POLR2A	chr3:50299898-50300330	MCF-7	breast:	n/a	n/a
6	POLR2A	chr3:50299909-50300286	K562	blood:	n/a	n/a
7	POLR2A	chr3:50299811-50301417	ECC-1	luminal epithelium:	n/a	n/a
8	POLR2A	chr3:50299678-50300770	HUVEC	blood vessel:	n/a	n/a
9	POLR2A	chr3:50299803-50300676	HUVEC	blood vessel:	n/a	n/a
10	POLR2A	chr3:50299905-50300182	MCF-7	breast:	n/a	n/a
11	POLR2A	chr3:50297997-50300909	K562	blood:	n/a	n/a
12	POLR2A	chr3:50300098-50300759	SK-N-MC	brain:	n/a	n/a
13	POLR2A	chr3:50300108-50300632	SK-N-SH	brain:	n/a	n/a

No data

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

No.	Distal block	Cell Line	Cell type
1	chr20:55796210..55799030-chr3:50298677..50300504,2	MCF-7	breast:
2	chr3:50296091..50300659-chr3:50356103..50362246,11	MCF-7	breast:
3	chr3:50299601..50302399-chr3:50309182..50311989,2	K562	blood:
4	chr3:50296030..50318456-chr3:50318822..50339499,66	MCF-7	breast:
5	chr3:50272655..50276499-chr3:50298744..50304497,10	MCF-7	breast:
6	chr3:50287507..50290097-chr3:50298834..50300693,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HYAL3-1	chr3:50297829-50300713	ENSG00000250212
2	lnc-GNAI2-1	chr3:50300083-50300495	NONHSAT089811

No data

Variant related genes	Relation type
SEMA3B	TF binding region
ENSG00000012171	Chromatin interaction
ENSG00000186792	Chromatin interaction
ENSG00000068001	Chromatin interaction
ENSG00000114353	Chromatin interaction
ENSG00000214706	Chromatin interaction
ENSG00000243477	Chromatin interaction

Extended variants
information (count: 77 )
Associated
traits (count: 4 )

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs10510755	0.93[CEU][hapmap]
rs1107265	0.82[MEX][hapmap]
rs11130248	0.81[CHD][hapmap]
rs12054403	0.81[CHB][hapmap];0.81[CHD][hapmap]
rs12485390	0.83[JPT][hapmap]
rs12488302	0.81[CHB][hapmap];0.81[CHD][hapmap]
rs12492880	0.81[CHD][hapmap]
rs12494414	0.86[CHD][hapmap];0.87[JPT][hapmap]
rs12629572	0.93[CEU][hapmap];0.89[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.87[MEX][hapmap];0.88[ASN][1000 genomes]
rs1989839	0.93[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.87[MEX][hapmap];0.83[ASN][1000 genomes]
rs2071203	0.81[CHD][hapmap]
rs2071204	0.81[CHD][hapmap]
rs2071802	0.93[CEU][hapmap]
rs2071803	0.93[CEU][hapmap]
rs2073498	0.87[CEU][hapmap]
rs2073499	1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.87[TSI][hapmap];0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2073500	0.81[CHD][hapmap]
rs2233474	1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.87[TSI][hapmap];0.80[AMR][1000 genomes];0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2233476	0.81[CHD][hapmap]
rs2236939	0.81[CEU][hapmap]
rs2236942	0.96[YRI][hapmap];0.90[AFR][1000 genomes]
rs2236944	0.81[CHD][hapmap]
rs2236946	0.81[CHD][hapmap];0.82[JPT][hapmap]
rs2236948	0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2236950	0.84[CHB][hapmap];0.85[CHD][hapmap];0.86[JPT][hapmap]
rs2236951	0.89[CHB][hapmap];0.90[CHD][hapmap];0.85[GIH][hapmap];0.95[JPT][hapmap];0.91[MEX][hapmap]
rs2236964	0.82[MEX][hapmap]
rs2239801	0.93[CEU][hapmap]
rs2282751	1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.90[TSI][hapmap];0.98[AMR][1000 genomes];0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2282753	0.82[MEX][hapmap]
rs2282754	0.82[MEX][hapmap]
rs2285043	0.81[CHD][hapmap]
rs2298953	0.81[CHD][hapmap]
rs2301639	0.93[CEU][hapmap]
rs28365992	0.93[CEU][hapmap]
rs3213621	0.81[CHD][hapmap]
rs35587949	0.81[CHD][hapmap]
rs3806708	0.93[CEU][hapmap]
rs4688682	0.83[JPT][hapmap]
rs4688732	0.81[CHD][hapmap]
rs4688734	0.81[CHD][hapmap]
rs57838764	0.83[ASN][1000 genomes]
rs6776145	0.93[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.87[MEX][hapmap];0.89[ASN][1000 genomes]
rs734767	0.82[MEX][hapmap]
rs739431	0.87[CEU][hapmap];0.96[GIH][hapmap];0.88[MKK][hapmap];0.87[TSI][hapmap];0.85[EUR][1000 genomes]
rs743757	0.82[MEX][hapmap]
rs762705	0.89[ASN][1000 genomes]
rs9852677	0.94[ASW][hapmap];0.85[CHB][hapmap];0.86[CHD][hapmap];0.81[GIH][hapmap];0.83[JPT][hapmap];0.91[LWK][hapmap];0.83[MEX][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes]
rs9883222	0.83[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:28 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1001775	chr3:50129479-50311666	Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
2	nsv523662	chr3:50144951-50584999	Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	101 gene(s)	inside rSNPs	diseases
3	nsv1013949	chr3:50151712-50339163	Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
4	nsv590250	chr3:50153356-50332697	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
5	nsv876769	chr3:50155468-50408398	Active TSS Enhancers Weak transcription Genic enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription 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	94 gene(s)	inside rSNPs	diseases
6	esv1821728	chr3:50156142-50657253	Strong transcription Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	109 gene(s)	inside rSNPs	diseases
7	esv1793751	chr3:50157364-50476363	Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	98 gene(s)	inside rSNPs	diseases
8	esv1828162	chr3:50157364-50506151	Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	98 gene(s)	inside rSNPs	diseases
9	nsv590251	chr3:50158774-50337422	Active TSS Strong transcription Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
10	nsv470561	chr3:50158774-50584999	Flanking Active TSS Enhancers Weak transcription Genic enhancers Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	99 gene(s)	inside rSNPs	diseases
11	nsv876770	chr3:50158774-50609624	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	103 gene(s)	inside rSNPs	diseases
12	nsv523560	chr3:50172397-50339163	Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
13	nsv460529	chr3:50178011-50324672	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
14	nsv460530	chr3:50178011-50324672	Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
15	nsv590252	chr3:50178011-50324672	Enhancers Bivalent Enhancer Strong transcription Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
16	nsv1002916	chr3:50187646-50311666	Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
17	nsv536564	chr3:50187646-50311666	Flanking Active TSS Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
18	nsv1014256	chr3:50187646-50339163	Enhancers Active TSS Strong transcription Weak transcription Genic enhancers Bivalent/Poised TSS Flanking Active 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	53 gene(s)	inside rSNPs	diseases
19	nsv536565	chr3:50187646-50339163	Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription Enhancers Weak transcription Genic enhancers 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	53 gene(s)	inside rSNPs	diseases
20	nsv1001993	chr3:50187646-50640808	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Strong transcription 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	104 gene(s)	inside rSNPs	diseases
21	nsv590253	chr3:50196418-50337422	Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
22	esv2757870	chr3:50198478-50371377	Genic enhancers Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	74 gene(s)	inside rSNPs	diseases
23	esv2759148	chr3:50198478-50371377	Enhancers Weak transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	74 gene(s)	inside rSNPs	diseases
24	nsv834692	chr3:50198485-50393464	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	94 gene(s)	inside rSNPs	diseases
25	nsv590254	chr3:50243510-50388607	Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	93 gene(s)	inside rSNPs	diseases
26	nsv460531	chr3:50247824-50436827	Strong transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	93 gene(s)	inside rSNPs	diseases
27	nsv590255	chr3:50247824-50436827	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	93 gene(s)	inside rSNPs	diseases
28	nsv876772	chr3:50255305-50436827	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	93 gene(s)	inside rSNPs	diseases

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs4141060	ZNF589	cis	cerebellum	SCAN
rs4141060	SLC25A20	cis	cerebellum	SCAN
rs4141060	TRAIP	cis	parietal	SCAN
rs4141060	PCBP4	cis	parietal	SCAN

Chromatin state (count:99 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:50284800-50300600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr3:50298200-50303400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr3:50298200-50304400	Enhancers	Ovary	ovary
4	chr3:50298400-50300200	Enhancers	Right Ventricle	heart
5	chr3:50298400-50301600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr3:50298400-50301800	Weak transcription	Aorta	Aorta
7	chr3:50298400-50303000	Weak transcription	Sigmoid Colon	Sigmoid Colon
8	chr3:50298600-50300400	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr3:50298600-50300400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr3:50298600-50301600	Weak transcription	HMEC	breast
11	chr3:50298600-50301800	Weak transcription	NHEK	skin
12	chr3:50298600-50302000	Weak transcription	Small Intestine	intestine
13	chr3:50298800-50300400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
14	chr3:50298800-50300600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
15	chr3:50298800-50300600	Enhancers	Skeletal Muscle Female	skeletal muscle
16	chr3:50298800-50301000	Weak transcription	H9 Cell Line	embryonic stem cell
17	chr3:50298800-50301000	Weak transcription	NHDF-Ad	bronchial
18	chr3:50298800-50301200	Weak transcription	K562	blood
19	chr3:50298800-50301600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr3:50298800-50301600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr3:50298800-50301600	Weak transcription	Gastric	stomach
22	chr3:50298800-50301800	Weak transcription	Rectal Mucosa Donor 31	rectum
23	chr3:50298800-50302000	Weak transcription	HUVEC	blood vessel
24	chr3:50298800-50302400	Weak transcription	Fetal Thymus	thymus
25	chr3:50298800-50302800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
26	chr3:50298800-50303200	Enhancers	Brain Anterior Caudate	brain
27	chr3:50298800-50303800	Enhancers	Brain Substantia Nigra	brain
28	chr3:50299000-50300200	Enhancers	Brain Angular Gyrus	brain
29	chr3:50299000-50300800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr3:50299000-50300800	Weak transcription	Placenta	Placenta
31	chr3:50299000-50301000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr3:50299000-50301000	Weak transcription	HUES6 Cell Line	embryonic stem cell
33	chr3:50299000-50301000	Weak transcription	HUES64 Cell Line	embryonic stem cell
34	chr3:50299000-50301000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
35	chr3:50299000-50301000	Weak transcription	A549	lung
36	chr3:50299000-50301400	Weak transcription	Fetal Intestine Large	intestine
37	chr3:50299000-50301600	Weak transcription	HUES48 Cell Line	embryonic stem cell
38	chr3:50299000-50301600	Weak transcription	Duodenum Smooth Muscle	Duodenum
39	chr3:50299000-50301600	Weak transcription	Rectal Mucosa Donor 29	rectum
40	chr3:50299000-50301600	Weak transcription	Stomach Mucosa	stomach
41	chr3:50299000-50301800	Weak transcription	Fetal Kidney	kidney
42	chr3:50299000-50302400	Weak transcription	Psoas Muscle	Psoas
43	chr3:50299000-50302600	Enhancers	Brain Hippocampus Middle	brain
44	chr3:50299000-50302600	Enhancers	Brain Inferior Temporal Lobe	brain
45	chr3:50299000-50303600	Enhancers	Brain Cingulate Gyrus	brain
46	chr3:50299000-50304400	Weak transcription	Liver	Liver
47	chr3:50299200-50300200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr3:50299200-50300200	Weak transcription	Brain Germinal Matrix	brain
49	chr3:50299200-50300400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
50	chr3:50299200-50300600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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