Variant report

Variant	nsv540643
Chromosome Location	chr10:57394631-57627820
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:559)
CpG islands
(count:61)
Chromatin interactive
region (count:7)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr10:57507840-57507889	K562	blood:	n/a	n/a
2	ATF2	chr10:57401358-57401696	GM12878	blood:	n/a	n/a
3	BATF	chr10:57518771-57519015	GM12878	blood:	n/a	chr10:57518959-57518970
4	BATF	chr10:57401376-57401698	GM12878	blood:	n/a	n/a
5	BATF	chr10:57518775-57519069	GM12878	blood:	n/a	chr10:57518959-57518970
6	BCL11A	chr10:57518766-57519117	GM12878	blood:	n/a	n/a
7	BCL11A	chr10:57401463-57401688	GM12878	blood:	n/a	chr10:57401610-57401619
8	BRCA1	chr10:57432975-57433057	Hela-S3	cervix:	n/a	n/a
9	BRCA1	chr10:57428118-57428215	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr10:57483653-57483898	IMR90	lung:	n/a	chr10:57483842-57483853
11	CEBPB	chr10:57552815-57553184	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr10:57394606-57394927	IMR90	lung:	n/a	chr10:57394769-57394780
13	CEBPB	chr10:57483591-57483950	A549	lung:	n/a	chr10:57483842-57483853
14	CEBPB	chr10:57560874-57561053	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr10:57493950-57494263	IMR90	lung:	n/a	chr10:57494109-57494118 chr10:57494109-57494118 chr10:57494107-57494118 chr10:57494109-57494118
16	CEBPB	chr10:57394713-57394811	K562	blood:	n/a	chr10:57394769-57394780
17	CEBPB	chr10:57493945-57494290	A549	lung:	n/a	chr10:57494109-57494118 chr10:57494109-57494118 chr10:57494107-57494118 chr10:57494109-57494118
18	CEBPB	chr10:57394611-57394911	A549	lung:	n/a	chr10:57394769-57394780
19	CEBPB	chr10:57400223-57400290	HepG2	liver:	n/a	n/a
20	CEBPB	chr10:57483522-57483901	H1-hESC	embryonic stem cell:	n/a	chr10:57483842-57483853
21	CEBPB	chr10:57506975-57507448	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr10:57495562-57495924	HepG2	liver:	n/a	n/a
23	CEBPB	chr10:57494052-57494186	H1-hESC	embryonic stem cell:	n/a	chr10:57494109-57494118 chr10:57494109-57494118 chr10:57494107-57494118 chr10:57494109-57494118
24	CEBPB	chr10:57394596-57394911	HepG2	liver:	n/a	chr10:57394769-57394780
25	CEBPB	chr10:57507027-57507291	HepG2	liver:	n/a	n/a
26	CEBPB	chr10:57483521-57483980	HepG2	liver:	n/a	chr10:57483842-57483853
27	CEBPB	chr10:57493973-57494246	HepG2	liver:	n/a	chr10:57494109-57494118 chr10:57494109-57494118 chr10:57494107-57494118 chr10:57494109-57494118
28	CEBPB	chr10:57512468-57512713	K562	blood:	n/a	n/a
29	CEBPB	chr10:57552760-57553149	A549	lung:	n/a	n/a
30	CEBPB	chr10:57512602-57512721	A549	lung:	n/a	n/a
31	CEBPZ	chr10:57480976-57481001	HepG2	liver:	n/a	n/a
32	CTCF	chr10:57500580-57500730	GM12875	blood:	n/a	n/a
33	CTCF	chr10:57427982-57428505	MCF-7	breast:	n/a	n/a
34	CTCF	chr10:57500619-57500800	HepG2	liver:	n/a	n/a
35	CTCF	chr10:57428119-57428414	SK-N-SH_RA	brain:	n/a	n/a
36	CTCF	chr10:57428200-57428350	GM12871	blood:	n/a	n/a
37	CTCF	chr10:57428220-57428370	NB4	blood:	n/a	n/a
38	CTCF	chr10:57428200-57428350	GM12878	blood:	n/a	n/a
39	CTCF	chr10:57500600-57500750	GM12873	blood:	n/a	n/a
40	CTCF	chr10:57500648-57500795	Kidney_OC	kidney:	n/a	n/a
41	CTCF	chr10:57555932-57555975	LNCaP	prostate:	n/a	n/a
42	CTCF	chr10:57428220-57428370	GM12875	blood:	n/a	n/a
43	CTCF	chr10:57500388-57501136	SK-N-SH	brain:	n/a	n/a
44	CTCF	chr10:57428220-57428370	HMEC	breast:	n/a	n/a
45	CTCF	chr10:57500620-57500770	GM12871	blood:	n/a	n/a
46	CTCF	chr10:57500634-57500745	HepG2	liver:	n/a	n/a
47	CTCF	chr10:57500640-57500790	NB4	blood:	n/a	n/a
48	CTCF	chr10:57500660-57500810	GM12874	blood:	n/a	n/a
49	CTCF	chr10:57500620-57500770	GM12867	blood:	n/a	n/a
50	CTCF	chr10:57428200-57428350	GM12874	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:57448681-57448731	MCF10A-Er-Src	breast:	n/a
2	chr10:57448681-57448731	HEEpiC	esophagus:	n/a
3	chr10:57448681-57448731	ECC-1	luminal epithelium:	n/a
4	chr10:57448681-57448731	AG04449	skin:	fetal
5	chr10:57448681-57448731	MCF-7	breast:	n/a
6	chr10:57448681-57448731	AoSMC	blood vessel:	n/a
7	chr10:57448681-57448731	NHDF-neo	bronchial:	n/a
8	chr10:57448681-57448731	HAEpiC	amniotic membrane:	n/a
9	chr10:57448681-57448731	NHBE	bronchial:	n/a
10	chr10:57448681-57448731	HRPEpiC	eye:	n/a
11	chr10:57448681-57448731	PFSK-1	brain:	n/a
12	chr10:57448681-57448731	NB4	blood:	n/a
13	chr10:57448681-57448731	HCM	heart:	n/a
14	chr10:57448681-57448731	HPAEpiC	pulmonary alveolar:	n/a
15	chr10:57448681-57448731	GM12892	blood:	n/a
16	chr10:57448681-57448731	HUVEC	blood vessel:	n/a
17	chr10:57448681-57448731	PrEC	prostate:	n/a
18	chr10:57448681-57448731	AG04450	lung:	fetal
19	chr10:57448681-57448731	GM12878	blood:	n/a
20	chr10:57448681-57448731	ProgFib	skin:	n/a
21	chr10:57448681-57448731	HNPCEpiC	eye:	n/a
22	chr10:57448681-57448731	IMR90	lung:	fetal
23	chr10:57448681-57448731	HEK293	kidney:	embryo
24	chr10:57448681-57448731	Jurkat	blood:	n/a
25	chr10:57448681-57448731	NH-A	brain:	n/a
26	chr10:57448681-57448731	RPTEC	kidney:	n/a
27	chr10:57448681-57448731	Caco-2	colon:	n/a
28	chr10:57448681-57448731	AG09309	skin:	n/a
29	chr10:57448681-57448731	SAEC	small airway:	n/a
30	chr10:57448681-57448731	ovcar-3	ovarian:	n/a
31	chr10:57448681-57448731	SK-N-SH_RA	brain:	n/a
32	chr10:57448681-57448731	Hela-S3	cervix:	n/a
33	chr10:57448681-57448731	SK-N-SH	brain:	n/a
34	chr10:57448681-57448731	HepG2	liver:	n/a
35	chr10:57448681-57448731	GM12891	blood:	n/a
36	chr10:57448681-57448731	H1-hESC	embryonic stem cell:	embryo
37	chr10:57448681-57448731	A549	lung:	n/a
38	chr10:57448681-57448731	Hepatocyte	liver:	n/a
39	chr10:57448681-57448731	CMK	blood:	n/a
40	chr10:57448681-57448731	PANC-1	pancreas:	n/a
41	chr10:57448681-57448731	HCPEpiC	choroid plexus:	n/a
42	chr10:57448681-57448731	HCF	heart:	n/a
43	chr10:57448681-57448731	BJ	skin:	n/a
44	chr10:57448681-57448731	HCT-116	colon:	n/a
45	chr10:57448681-57448731	HRCEpiC	kidney:	n/a
46	chr10:57448681-57448731	HIPEpiC	eye:	n/a
47	chr10:57448681-57448731	GM19239	blood:	n/a
48	chr10:57448681-57448731	T-47D	breast:	n/a
49	chr10:57448681-57448731	LNCaP	prostate:	n/a
50	chr10:57448681-57448731	AG10803	skin:	n/a

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No.	Distal block	Cell Line	Cell type
1	chr10:57409945..57412041-chr10:57413337..57415798,2	K562	blood:
2	chr10:55961337..55963211-chr10:57586910..57589588,2	K562	blood:
3	chr10:57624031..57627084-chr10:57627386..57630706,3	K562	blood:
4	chr10:57624031..57627084-chr10:57627386..57630706,3	K562	blood:
5	chr10:57475413..57477793-chr10:57482048..57484055,2	K562	blood:
6	chr10:57409945..57412041-chr10:57413337..57415798,2	K562	blood:
7	chr10:57475413..57477793-chr10:57482048..57484055,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MTRNR2L5-5	chr10:57506311-57506668	NONHSAT013465

No data

Variant related genes	Relation type
GAPDHP21	TF binding region
ENSG00000270541	TF binding region
GAPDHP21	CpG island
ENSG00000270541	CpG island

Extended variants
information (count: 1940 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:1940 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs566984612	chr10:57402081-57402082	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs545101697	chr10:57402157-57402158	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs111476620	chr10:57402188-57402189	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs527782953	chr10:57402197-57402198	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs76321272	chr10:57402201-57402202	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs200398942	chr10:57402203-57402204	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs530802922	chr10:57402218-57402219	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs544640084	chr10:57402306-57402307	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs113295581	chr10:57402307-57402308	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs561002591	chr10:57402342-57402343	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs530050224	chr10:57402382-57402383	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs184130852	chr10:57402394-57402395	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs188900493	chr10:57402395-57402396	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs566615215	chr10:57408659-57408660	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs551589913	chr10:57408671-57408672	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs552184444	chr10:57408682-57408683	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs12248551	chr10:57408686-57408687	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs537770102	chr10:57408690-57408691	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs140552085	chr10:57408710-57408711	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs573887706	chr10:57408723-57408724	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs536496192	chr10:57408756-57408757	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs114258465	chr10:57408758-57408759	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs188442138	chr10:57413400-57413401	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs16907581	chr10:57413435-57413436	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs558350021	chr10:57413452-57413453	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs16907583	chr10:57413456-57413457	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs2461897	chr10:57413461-57413462	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs193055146	chr10:57413523-57413524	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs369974461	chr10:57413594-57413595	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs112803383	chr10:57413714-57413715	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs184263792	chr10:57413740-57413741	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs528971906	chr10:57413759-57413760	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs139098312	chr10:57413775-57413776	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs149445443	chr10:57413790-57413791	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs559351468	chr10:57413861-57413862	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs528409449	chr10:57413923-57413924	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs368888240	chr10:57413933-57413934	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs375584294	chr10:57426424-57426425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs576599250	chr10:57426438-57426439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs12256296	chr10:57426446-57426447	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs11004953	chr10:57426519-57426520	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs562067897	chr10:57426529-57426530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs2177365	chr10:57426592-57426593	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs182193631	chr10:57426641-57426642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs140807401	chr10:57426668-57426669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs533058021	chr10:57426671-57426672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs527906794	chr10:57426683-57426684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs150140774	chr10:57426687-57426688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs138719109	chr10:57426691-57426692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs2392949	chr10:57426710-57426711	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:63)

Disease	PMID	Source
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	18632612	CNVD
Autism	18414403	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
T-cell lymphomas	19863542	CNVD
Testicular germ cell tumor	18059402	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Obesity	21956041	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16272173	CNVD
Metanephric adenoma	20802469	CNVD
Autism	20841430	CNVD
Mental retardation	17124404	CNVD
Epilepsy	20923578	CNVD
Prostate cancer	16573809	CNVD
Schizophrenia	19329560	CNVD
Heart failure	18772530	CNVD
Heart failure	18854381	CNVD
Hyperglycemia	19060297	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Glioblastoma multiforme	22286061	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Usher syndrome	20538994	CNVD
Glioblastoma multiforme	17002787	CNVD
Autism	20858243	CNVD
Cancer	20164919	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
small cell lung cancer	17426248	CNVD

Chromatin state (count:135 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:57402000-57402400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr10:57408600-57408800	Enhancers	Gastric	stomach
3	chr10:57413400-57413800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr10:57413400-57414000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr10:57426400-57428600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr10:57427400-57427600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr10:57428200-57430400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr10:57430200-57430600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr10:57430400-57430800	Enhancers	Primary hematopoietic stem cells	blood
10	chr10:57463600-57464200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr10:57463800-57464800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr10:57464400-57464800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
13	chr10:57483400-57484000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr10:57496600-57497000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr10:57496600-57497000	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr10:57496600-57497000	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr10:57496600-57497000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr10:57496600-57497200	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr10:57496600-57497200	Enhancers	iPS-15b Cell Line	embryonic stem cell
20	chr10:57496600-57497400	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chr10:57497000-57499600	Weak transcription	HUES64 Cell Line	embryonic stem cell
22	chr10:57497000-57499600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr10:57497200-57499600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
24	chr10:57497400-57499600	Weak transcription	HUES6 Cell Line	embryonic stem cell
25	chr10:57499400-57500200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr10:57499600-57499800	Enhancers	HUES64 Cell Line	embryonic stem cell
27	chr10:57499600-57499800	Enhancers	Pancreas	Pancrea
28	chr10:57499600-57500000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr10:57499600-57500400	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr10:57499600-57500400	Enhancers	Fetal Heart	heart
31	chr10:57499600-57500800	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr10:57499600-57501000	Enhancers	Liver	Liver
33	chr10:57499800-57500200	Enhancers	HepG2	liver
34	chr10:57500000-57500200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr10:57500800-57506800	Weak transcription	HUES6 Cell Line	embryonic stem cell
36	chr10:57501000-57506200	Weak transcription	Liver	Liver
37	chr10:57506200-57507400	Enhancers	Liver	Liver
38	chr10:57506400-57507600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr10:57506600-57507600	Enhancers	H1 Cell Line	embryonic stem cell
40	chr10:57506600-57507600	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr10:57506800-57507400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr10:57506800-57507400	Enhancers	HUES64 Cell Line	embryonic stem cell
43	chr10:57506800-57507400	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr10:57506800-57507600	Enhancers	H9 Cell Line	embryonic stem cell
45	chr10:57506800-57507600	Enhancers	HUES6 Cell Line	embryonic stem cell
46	chr10:57506800-57507600	Enhancers	iPS-18 Cell Line	embryonic stem cell
47	chr10:57506800-57507800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr10:57507000-57507600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
49	chr10:57527800-57528400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr10:57528000-57528400	Enhancers	HUES48 Cell Line	embryonic stem cell

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