Variant report

Variant	nsv581335
Chromosome Location	chr2:34061344-34163414
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:214)
CpG islands
(count:183)
Chromatin interactive
region (count:1)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:214 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr2:34154420-34154896	GM12878	blood:	n/a	n/a
2	BHLHE40	chr2:34118559-34118568	GM12878	blood:	n/a	n/a
3	CEBPB	chr2:34135044-34135347	A549	lung:	n/a	chr2:34135192-34135203
4	CEBPB	chr2:34151939-34152080	HepG2	liver:	n/a	chr2:34152019-34152030
5	CEBPB	chr2:34074371-34074506	H1-hESC	embryonic stem cell:	n/a	chr2:34074408-34074419
6	CEBPB	chr2:34074246-34074592	IMR90	lung:	n/a	chr2:34074408-34074419
7	CEBPB	chr2:34134997-34135391	HepG2	liver:	n/a	chr2:34135192-34135203
8	CEBPB	chr2:34135027-34135284	HepG2	liver:	n/a	chr2:34135192-34135203
9	CEBPB	chr2:34063261-34063570	HepG2	liver:	n/a	chr2:34063436-34063447
10	CEBPB	chr2:34135074-34135413	HepG2	liver:	n/a	chr2:34135192-34135203
11	CEBPB	chr2:34135075-34135323	MCF-7	breast:	n/a	chr2:34135192-34135203
12	CEBPB	chr2:34130752-34130767	HepG2	liver:	n/a	chr2:34130752-34130763
13	CEBPB	chr2:34063300-34063564	IMR90	lung:	n/a	chr2:34063436-34063447
14	CEBPB	chr2:34074255-34074588	HepG2	liver:	n/a	chr2:34074408-34074419
15	CEBPB	chr2:34074263-34074579	A549	lung:	n/a	chr2:34074408-34074419
16	CEBPB	chr2:34098418-34098628	A549	lung:	n/a	n/a
17	CEBPB	chr2:34135031-34135356	IMR90	lung:	n/a	chr2:34135192-34135203
18	CEBPB	chr2:34062064-34062078	HepG2	liver:	n/a	n/a
19	CEBPB	chr2:34147478-34147805	HepG2	liver:	n/a	chr2:34147619-34147630
20	CEBPB	chr2:34135002-34135429	MCF-7	breast:	n/a	chr2:34135192-34135203
21	CEBPB	chr2:34093496-34093707	A549	lung:	n/a	n/a
22	CEBPB	chr2:34090949-34090976	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr2:34152960-34153250	A549	lung:	n/a	n/a
24	CEBPB	chr2:34135064-34135307	H1-hESC	embryonic stem cell:	n/a	chr2:34135192-34135203
25	CEBPB	chr2:34135009-34135391	HepG2	liver:	n/a	chr2:34135192-34135203
26	CEBPB	chr2:34153006-34153284	HepG2	liver:	n/a	n/a
27	CEBPB	chr2:34062049-34062067	A549	lung:	n/a	n/a
28	CEBPB	chr2:34135017-34135373	Hela-S3	cervix:	n/a	chr2:34135192-34135203
29	CEBPB	chr2:34073519-34074040	IMR90	lung:	n/a	n/a
30	CEBPD	chr2:34135044-34135328	HepG2	liver:	n/a	n/a
31	CREB1	chr2:34154589-34154875	GM12878	blood:	n/a	n/a
32	CTCF	chr2:34161636-34161692	GM20000	blood:	n/a	n/a
33	CTCF	chr2:34111880-34112030	WERI-Rb-1	eye:	n/a	n/a
34	CTCF	chr2:34085662-34085749	LNCaP	prostate:	n/a	n/a
35	CTCF	chr2:34067320-34067470	HFF	foreskin:	n/a	n/a
36	CTCF	chr2:34084463-34084530	Lung_OC	lung:	n/a	n/a
37	CTCF	chr2:34067392-34067445	Gliobla	brain:	n/a	n/a
38	CTCF	chr2:34111900-34112050	Hela-S3	cervix:	n/a	n/a
39	CTCF	chr2:34160121-34160192	Medullo	brain:	n/a	n/a
40	CTCF	chr2:34063595-34063608	GM13976	blood:	n/a	n/a
41	CTCF	chr2:34140857-34140899	LNCaP	prostate:	n/a	n/a
42	CTCF	chr2:34104940-34105090	GM12864	blood:	n/a	n/a
43	CTCF	chr2:34067260-34067410	HepG2	liver:	n/a	n/a
44	CTCF	chr2:34067220-34067370	MCF-7	breast:	n/a	n/a
45	CTCF	chr2:34067280-34067430	HEK293	kidney:	n/a	n/a
46	CTCF	chr2:34065014-34065083	Lung_OC	lung:	n/a	n/a
47	CTCF	chr2:34067380-34067530	A549	lung:	n/a	n/a
48	CTCF	chr2:34123480-34123630	GM12868	blood:	n/a	n/a
49	CTCF	chr2:34067340-34067490	GM12873	blood:	n/a	n/a
50	CTCF	chr2:34064988-34065081	MCF-7	breast:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:34128909-34128959	CMK	blood:	n/a
2	chr2:34128696-34128746	H1-hESC	embryonic stem cell:	embryo
3	chr2:34128696-34128746	LNCaP	prostate:	n/a
4	chr2:34128696-34128746	GM12891	blood:	n/a
5	chr2:34128722-34128772	MCF10A-Er-Src	breast:	n/a
6	chr2:34128696-34128746	HEEpiC	esophagus:	n/a
7	chr2:34128696-34128746	AG10803	skin:	n/a
8	chr2:34128696-34128746	HUVEC	blood vessel:	n/a
9	chr2:34128722-34128772	AG09319	gingival:	n/a
10	chr2:34128909-34128959	AG09309	skin:	n/a
11	chr2:34128722-34128772	AG09309	skin:	n/a
12	chr2:34128696-34128746	SK-N-SH_RA	brain:	n/a
13	chr2:34128909-34128959	Hela-S3	cervix:	n/a
14	chr2:34128696-34128746	AG09319	gingival:	n/a
15	chr2:34128909-34128959	GM12891	blood:	n/a
16	chr2:34128722-34128772	BJ	skin:	n/a
17	chr2:34128909-34128959	Caco-2	colon:	n/a
18	chr2:34128696-34128746	PANC-1	pancreas:	n/a
19	chr2:34128696-34128746	A549	lung:	n/a
20	chr2:34128909-34128959	A549	lung:	n/a
21	chr2:34128722-34128772	PANC-1	pancreas:	n/a
22	chr2:34128696-34128746	RPTEC	kidney:	n/a
23	chr2:34128722-34128772	Jurkat	blood:	n/a
24	chr2:34128696-34128746	AoSMC	blood vessel:	n/a
25	chr2:34128696-34128746	HCPEpiC	choroid plexus:	n/a
26	chr2:34128696-34128746	NH-A	brain:	n/a
27	chr2:34128696-34128746	HCM	heart:	n/a
28	chr2:34128722-34128772	GM12878	blood:	n/a
29	chr2:34128696-34128746	HPAEpiC	pulmonary alveolar:	n/a
30	chr2:34128722-34128772	NT2-D1	testis:	n/a
31	chr2:34128722-34128772	HRE	kidney:	n/a
32	chr2:34128696-34128746	ECC-1	luminal epithelium:	n/a
33	chr2:34128909-34128959	U87	brain:	n/a
34	chr2:34128722-34128772	Caco-2	colon:	n/a
35	chr2:34128909-34128959	NHDF-neo	bronchial:	n/a
36	chr2:34128722-34128772	A549	lung:	n/a
37	chr2:34128722-34128772	BE2_C	brain:	n/a
38	chr2:34128909-34128959	K562	blood:	n/a
39	chr2:34128909-34128959	NHBE	bronchial:	n/a
40	chr2:34128722-34128772	PFSK-1	brain:	n/a
41	chr2:34128696-34128746	Caco-2	colon:	n/a
42	chr2:34128722-34128772	ProgFib	skin:	n/a
43	chr2:34128696-34128746	NB4	blood:	n/a
44	chr2:34128722-34128772	HepG2	liver:	n/a
45	chr2:34128722-34128772	AG04449	skin:	fetal
46	chr2:34128909-34128959	HepG2	liver:	n/a
47	chr2:34128696-34128746	Jurkat	blood:	n/a
48	chr2:34128722-34128772	K562	blood:	n/a
49	chr2:34128909-34128959	BJ	skin:	n/a
50	chr2:34128722-34128772	H1-hESC	embryonic stem cell:	embryo

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:34160770..34163344-chr2:34168919..34171059,2	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RASGRP3-1	chr2:34080755-34080820	ENSG00000203386
2	lnc-RASGRP3-1	chr2:34151907-34152035	ENSG00000203386
3	lnc-RASGRP3-1	chr2:34080755-34080820	ENSG00000203386
4	lnc-RASGRP3-12	chr2:34145797-34145874	NONHSAT070029
5	lnc-RASGRP3-1	chr2:34111439-34111541	ENSG00000203386
6	lnc-RASGRP3-12	chr2:34147670-34148121	NONHSAT070029
7	lnc-RASGRP3-12	chr2:34146785-34146851	NONHSAT070029
8	lnc-RASGRP3-1	chr2:34151907-34152035	ENSG00000203386

No data

Variant related genes	Relation type
SLC25A5P2	TF binding region
ENSG00000266861	TF binding region
SLC25A5P2	CpG island
ENSG00000266861	CpG island

Extended variants
information (count: 2176 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:2176 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11695787	chr2:34061344-34061345	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs10198829	chr2:34061367-34061368	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs530199635	chr2:34061375-34061376	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs550336390	chr2:34061415-34061416	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs185290845	chr2:34061417-34061418	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs374939132	chr2:34061440-34061441	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs72864620	chr2:34061444-34061445	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs191925676	chr2:34061505-34061506	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs72864623	chr2:34061507-34061508	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs566210899	chr2:34061547-34061548	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs535351723	chr2:34061550-34061551	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs556058116	chr2:34061589-34061590	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs554721673	chr2:34061598-34061599	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs574725481	chr2:34061621-34061622	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs183290688	chr2:34061675-34061676	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs189132195	chr2:34061685-34061686	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs144897640	chr2:34061688-34061689	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs577746420	chr2:34061721-34061722	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs576880530	chr2:34061738-34061739	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs545447499	chr2:34061741-34061742	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs559321253	chr2:34061742-34061743	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs573030545	chr2:34061773-34061774	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs884874	chr2:34061790-34061791	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs561853278	chr2:34061799-34061800	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs546996732	chr2:34064821-34064822	Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs567187372	chr2:34064827-34064828	Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs78439732	chr2:34064839-34064840	Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs181203869	chr2:34064863-34064864	Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs113510688	chr2:34064881-34064882	Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs79200953	chr2:34064900-34064901	Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs369387361	chr2:34064901-34064902	Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs80225995	chr2:34064911-34064912	Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs543084273	chr2:34064917-34064918	Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs113554814	chr2:34064948-34064949	Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs373682267	chr2:34064951-34064952	Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs112152675	chr2:34064952-34064953	Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs77036686	chr2:34064959-34064960	Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs114296479	chr2:34064969-34064970	Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs76541366	chr2:34064980-34064981	Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs116567172	chr2:34064984-34064985	Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs79564932	chr2:34065001-34065002	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs532111105	chr2:34065005-34065006	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs547969955	chr2:34065007-34065008	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs202243559	chr2:34065026-34065027	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs112829838	chr2:34065035-34065036	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs576605402	chr2:34065043-34065044	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs545587299	chr2:34065081-34065082	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs186908721	chr2:34065088-34065089	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs191796279	chr2:34065089-34065090	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs144184651	chr2:34065104-34065105	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Bladder cancer	21909424	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	19521722	CNVD
Autism	18522746	CNVD
Breast cancer	21364760	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	18927303	CNVD
Hereditary gingival fibromatosis	19633868	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Prostate cancer	21965145	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
Neurocytoma	17123091	CNVD
Autism	22495309	CNVD
Schizophrenia	23813976	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD

Chromatin state (count:105 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:34061000-34061800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr2:34064800-34065200	Active TSS	Brain Substantia Nigra	brain
3	chr2:34065000-34065200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr2:34065600-34065800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr2:34065800-34072000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr2:34069600-34070000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr2:34070000-34072600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr2:34072600-34076000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr2:34073000-34074600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr2:34073000-34074600	Enhancers	NHDF-Ad	bronchial
11	chr2:34073200-34074200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr2:34073200-34074400	Enhancers	NH-A	brain
13	chr2:34073400-34074200	Enhancers	HUES64 Cell Line	embryonic stem cell
14	chr2:34073400-34074200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr2:34073400-34074200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr2:34074200-34075200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr2:34075200-34075800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr2:34078200-34078800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
19	chr2:34080000-34082200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr2:34080400-34087800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr2:34082200-34082400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr2:34082200-34082400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr2:34082400-34085000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr2:34084400-34085000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr2:34084400-34085000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr2:34084400-34085800	Enhancers	Dnd41	blood
27	chr2:34084600-34084800	Enhancers	Cortex derived primary cultured neurospheres	brain
28	chr2:34084600-34085000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
29	chr2:34084600-34085000	Enhancers	Ovary	ovary
30	chr2:34084600-34085600	Enhancers	Primary hematopoietic stem cells short term culture	blood
31	chr2:34084600-34085800	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr2:34084800-34085400	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
33	chr2:34084800-34085600	Enhancers	iPS-20b Cell Line	embryonic stem cell
34	chr2:34084800-34085600	Enhancers	Primary monocytes fromperipheralblood	blood
35	chr2:34085000-34085200	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr2:34085000-34085200	Enhancers	Brain Cingulate Gyrus	brain
37	chr2:34085000-34085200	Enhancers	Brain Substantia Nigra	brain
38	chr2:34085000-34085200	Enhancers	Fetal Lung	lung
39	chr2:34085000-34085200	Flanking Active TSS	Ovary	ovary
40	chr2:34085000-34085400	Enhancers	H1 Cell Line	embryonic stem cell
41	chr2:34085000-34085400	Active TSS	Primary B cells from cord blood	blood
42	chr2:34085000-34085400	Enhancers	Fetal Muscle Leg	muscle
43	chr2:34085000-34085400	Enhancers	Right Atrium	heart
44	chr2:34085000-34085600	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr2:34085000-34085600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr2:34085000-34085600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr2:34085000-34085600	Active TSS	Brain Anterior Caudate	brain
48	chr2:34085000-34085800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr2:34085000-34086400	Enhancers	HUES48 Cell Line	embryonic stem cell
50	chr2:34085200-34085400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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