Variant report

Variant	nsv1017249
Chromosome Location	chr6:62906813-63317382
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:863)
CpG islands
(count:1100)
Chromatin interactive
region (count:7)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:863 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr6:63008621-63009133	GM12878	blood:	n/a	n/a
2	ATF2	chr6:63008561-63009076	GM12878	blood:	n/a	n/a
3	ATF2	chr6:63077568-63077881	GM12878	blood:	n/a	n/a
4	BACH1	chr6:63036580-63036810	H1-hESC	embryonic stem cell:	n/a	chr6:63036749-63036763
5	BACH1	chr6:63275845-63276042	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr6:62995853-62996194	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr6:62996403-62996585	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr6:62964878-62964884	K562	blood:	n/a	n/a
9	BCL11A	chr6:63008564-63009026	GM12878	blood:	n/a	n/a
10	BCL11A	chr6:63261207-63261405	GM12878	blood:	n/a	n/a
11	BCL3	chr6:63008674-63008913	GM12878	blood:	n/a	n/a
12	BCLAF1	chr6:63008581-63009054	GM12878	blood:	n/a	n/a
13	BHLHE40	chr6:63115576-63115579	GM12878	blood:	n/a	n/a
14	BHLHE40	chr6:63008716-63009043	GM12878	blood:	n/a	n/a
15	BRCA1	chr6:63297856-63298053	H1-hESC	embryonic stem cell:	n/a	n/a
16	CCNT2	chr6:63244049-63244248	K562	blood:	n/a	n/a
17	CEBPB	chr6:63234202-63234462	HepG2	liver:	n/a	n/a
18	CEBPB	chr6:63195602-63195944	HepG2	liver:	n/a	chr6:63195781-63195792
19	CEBPB	chr6:63184716-63185068	HepG2	liver:	n/a	chr6:63184880-63184891
20	CEBPB	chr6:63200426-63200489	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr6:63007513-63007781	H1-hESC	embryonic stem cell:	n/a	chr6:63007660-63007671
22	CEBPB	chr6:62990637-62990985	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr6:62944204-62944407	HepG2	liver:	n/a	chr6:62944258-62944269
24	CEBPB	chr6:62922451-62922713	HepG2	liver:	n/a	chr6:62922558-62922569
25	CEBPB	chr6:63311156-63311399	A549	lung:	n/a	n/a
26	CEBPB	chr6:63184706-63185048	ECC-1	luminal epithelium:	n/a	chr6:63184880-63184891
27	CEBPB	chr6:63195619-63195937	IMR90	lung:	n/a	chr6:63195781-63195792
28	CEBPB	chr6:62946841-62947210	HepG2	liver:	n/a	chr6:62947127-62947138
29	CEBPB	chr6:63216022-63216260	HepG2	liver:	n/a	chr6:63216135-63216146 chr6:63216135-63216148 chr6:63216132-63216149
30	CEBPB	chr6:62946833-62947208	IMR90	lung:	n/a	chr6:62947127-62947138
31	CEBPB	chr6:63316649-63316921	HepG2	liver:	n/a	n/a
32	CEBPB	chr6:63085265-63085473	HepG2	liver:	n/a	n/a
33	CEBPB	chr6:63007518-63007799	HepG2	liver:	n/a	chr6:63007660-63007671
34	CEBPB	chr6:63311181-63311407	MCF-7	breast:	n/a	n/a
35	CEBPB	chr6:63186918-63187244	HepG2	liver:	n/a	chr6:63187071-63187082
36	CEBPB	chr6:63184778-63185113	ECC-1	luminal epithelium:	n/a	chr6:63184880-63184891
37	CEBPB	chr6:63001581-63001758	IMR90	lung:	n/a	n/a
38	CEBPB	chr6:62946882-62947198	H1-hESC	embryonic stem cell:	n/a	chr6:62947127-62947138
39	CEBPB	chr6:62922422-62922696	Hela-S3	cervix:	n/a	chr6:62922558-62922569
40	CEBPB	chr6:62946881-62947231	A549	lung:	n/a	chr6:62947127-62947138
41	CEBPB	chr6:62922410-62922634	H1-hESC	embryonic stem cell:	n/a	chr6:62922558-62922569
42	CEBPB	chr6:63176620-63176650	HepG2	liver:	n/a	n/a
43	CEBPB	chr6:63165587-63165869	IMR90	lung:	n/a	n/a
44	CEBPB	chr6:63072299-63072645	HepG2	liver:	n/a	chr6:63072437-63072450 chr6:63072437-63072450 chr6:63072438-63072449 chr6:63072628-63072641
45	CEBPB	chr6:63184708-63185066	IMR90	lung:	n/a	chr6:63184880-63184891
46	CEBPB	chr6:63184719-63185081	H1-hESC	embryonic stem cell:	n/a	chr6:63184880-63184891
47	CEBPB	chr6:63184713-63185024	A549	lung:	n/a	chr6:63184880-63184891
48	CEBPB	chr6:62993180-62993341	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr6:63195679-63195883	H1-hESC	embryonic stem cell:	n/a	chr6:63195781-63195792
50	CEBPB	chr6:62925564-62925677	HepG2	liver:	n/a	chr6:62925642-62925653

(count:1100 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:62995523-62995573	HCF	heart:	n/a
2	chr6:63038652-63038702	SK-N-SH	brain:	n/a
3	chr6:62995523-62995573	HCF	heart:	n/a
4	chr6:63038652-63038702	SK-N-SH	brain:	n/a
5	chr6:62996627-62996677	SK-N-SH	brain:	n/a
6	chr6:62995876-62995926	NH-A	brain:	n/a
7	chr6:62996183-62996233	PFSK-1	brain:	n/a
8	chr6:62996299-62996349	NHBE	bronchial:	n/a
9	chr6:62996132-62996182	GM19239	blood:	n/a
10	chr6:62996132-62996182	AG09309	skin:	n/a
11	chr6:62996627-62996677	NH-A	brain:	n/a
12	chr6:62996130-62996180	BJ	skin:	n/a
13	chr6:62996627-62996677	Caco-2	colon:	n/a
14	chr6:62996697-62996747	MCF-7	breast:	n/a
15	chr6:63157784-63157834	HEEpiC	esophagus:	n/a
16	chr6:62995876-62995926	NT2-D1	testis:	n/a
17	chr6:62995876-62995926	NHBE	bronchial:	n/a
18	chr6:62996299-62996349	PANC-1	pancreas:	n/a
19	chr6:62995523-62995573	NH-A	brain:	n/a
20	chr6:62996664-62996714	HEK293	kidney:	embryo
21	chr6:63226373-63226423	HMEC	breast:	n/a
22	chr6:62996697-62996747	HCT-116	colon:	n/a
23	chr6:62996214-62996264	SKMC	muscle:	n/a
24	chr6:62996183-62996233	HRCEpiC	kidney:	n/a
25	chr6:62996214-62996264	SAEC	small airway:	n/a
26	chr6:62995523-62995573	Hela-S3	cervix:	n/a
27	chr6:62996183-62996233	LNCaP	prostate:	n/a
28	chr6:62996627-62996677	RPTEC	kidney:	n/a
29	chr6:62995523-62995573	GM12892	blood:	n/a
30	chr6:62996697-62996747	HRPEpiC	eye:	n/a
31	chr6:62996022-62996072	SK-N-SH_RA	brain:	n/a
32	chr6:62996022-62996072	NB4	blood:	n/a
33	chr6:62996119-62996169	IMR90	lung:	fetal
34	chr6:62996627-62996677	ECC-1	luminal epithelium:	n/a
35	chr6:62996627-62996677	MCF10A-Er-Src	breast:	n/a
36	chr6:62995963-62996013	HCT-116	colon:	n/a
37	chr6:62996214-62996264	Hela-S3	cervix:	n/a
38	chr6:63157784-63157834	HNPCEpiC	eye:	n/a
39	chr6:62995963-62996013	BJ	skin:	n/a
40	chr6:62996183-62996233	GM12892	blood:	n/a
41	chr6:62996702-62996752	SK-N-MC	brain:	n/a
42	chr6:62976042-62976092	PANC-1	pancreas:	n/a
43	chr6:62996664-62996714	BE2_C	brain:	n/a
44	chr6:62996627-62996677	HAEpiC	amniotic membrane:	n/a
45	chr6:62995523-62995573	HCT-116	colon:	n/a
46	chr6:62995963-62996013	IMR90	lung:	fetal
47	chr6:62976042-62976092	MCF-7	breast:	n/a
48	chr6:62996022-62996072	HL-60	blood:	n/a
49	chr6:62995876-62995926	U87	brain:	n/a
50	chr6:62996022-62996072	HMEC	breast:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:63278592..63281366-chr6:63283322..63285509,2	MCF-7	breast:
2	chr6:63211094..63213340-chr6:63214100..63215970,2	MCF-7	breast:
3	chr6:63211094..63213340-chr6:63214100..63215970,2	MCF-7	breast:
4	chr6:63278592..63281366-chr6:63283322..63285509,2	MCF-7	breast:
5	chr1:28560124..28560625-chr6:63259614..63260114,2	NB4	blood:
6	chr6:62973850..62974714-chr7:113350282..113350966,2	MCF-7	breast:
7	chr6:62518763..62519292-chr6:62993656..62994388,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FKBP1C-2	chr6:63257332-63257472	NONHSAT113334
2	lnc-FKBP1C-2	chr6:63257927-63258177	NONHSAT113334
3	lnc-KHDRBS2-3	chr6:63297418-63297607	NONHSAT113335
4	lnc-KHDRBS2-2	chr6:63170845-63171408	NONHSAT113333
5	lnc-KHDRBS2-3	chr6:63298023-63298059	NONHSAT113335

No data

Variant related genes	Relation type
KHDRBS2	TF binding region
ENSG00000217067	TF binding region
ENSG00000216859	TF binding region
KHDRBS2	CpG island
ENSG00000217067	CpG island
ENSG00000216859	CpG island

Extended variants
information (count: 6850 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:6850 , 50 per page) page: 1 2 3 4 5 6 7 ... 137

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs368197975	chr6:62911218-62911219	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs532671358	chr6:62911226-62911227	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs192809197	chr6:62911282-62911283	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs570721101	chr6:62911347-62911348	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs563119824	chr6:62911442-62911443	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs150730449	chr6:62911473-62911474	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs530329763	chr6:62911527-62911528	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs541058008	chr6:62911549-62911550	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs184671607	chr6:62911560-62911561	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs139024475	chr6:62911565-62911566	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs187570241	chr6:62911616-62911617	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs566125496	chr6:62911692-62911693	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs536462396	chr6:62911718-62911719	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs555119715	chr6:62911739-62911740	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs71568790	chr6:62911772-62911773	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs116192781	chr6:62911773-62911774	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs192514956	chr6:62911780-62911781	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs149913416	chr6:62911781-62911782	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs528043129	chr6:62911792-62911793	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs141309842	chr6:62921604-62921605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs150342263	chr6:62921668-62921669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs567689	chr6:62921711-62921712	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs528684364	chr6:62921761-62921762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs556970314	chr6:62921776-62921777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs576360114	chr6:62921802-62921803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs575224817	chr6:62921812-62921813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs185619459	chr6:62921813-62921814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs138095713	chr6:62921877-62921878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs149525673	chr6:62921959-62921960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs543781697	chr6:62921990-62921991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs562391522	chr6:62921995-62921996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs529643775	chr6:62922014-62922015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs544906996	chr6:62922017-62922018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs562510418	chr6:62922021-62922022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs532942155	chr6:62922078-62922079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs562087976	chr6:62922082-62922083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs370889202	chr6:62922084-62922085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs542522678	chr6:62922108-62922109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs527514334	chr6:62922122-62922123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs548792376	chr6:62922129-62922130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs143029000	chr6:62922218-62922219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs562188789	chr6:62922230-62922231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs529741464	chr6:62922240-62922241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs77380545	chr6:62922310-62922311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs549661170	chr6:62922338-62922339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs484791	chr6:62922423-62922424	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs485617	chr6:62922474-62922475	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs557986507	chr6:62922501-62922502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs527449822	chr6:62922575-62922576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs573260812	chr6:62922584-62922585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:76)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastric cancer	17908304	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Systemic lupus erythematosus	17503323	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Cancer	21637783	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Oral squamous cell carcinoma	17134496	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Lung cancer	19547694	CNVD
Myelofibrosis	22110671	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Ependymoma	16718352	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	23813976	CNVD
Tetralogy of Fallot	22912587	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Pancreatic cancer	17952125	CNVD
Autism	19492091	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	20164920	CNVD

Chromatin state (count:636 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:62911200-62911600	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr6:62911200-62911800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr6:62921600-62929600	Weak transcription	Primary B cells from cord blood	blood
4	chr6:62922800-62923200	Active TSS	A549	lung
5	chr6:62923000-62923400	Enhancers	Hela-S3	cervix
6	chr6:62923200-62923400	Flanking Active TSS	A549	lung
7	chr6:62925200-62925400	Active TSS	Ovary	ovary
8	chr6:62932600-62933400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
9	chr6:62933400-62933800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr6:62937200-62939200	Weak transcription	H1 Cell Line	embryonic stem cell
11	chr6:62938800-62939200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr6:62938800-62939800	ZNF genes & repeats	Fetal Intestine Small	intestine
13	chr6:62939000-62939200	Enhancers	Gastric	stomach
14	chr6:62939000-62939400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr6:62939200-62939600	Strong transcription	H1 Cell Line	embryonic stem cell
16	chr6:62939200-62939600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr6:62939200-62939600	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr6:62939600-62939800	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
19	chr6:62939600-62941000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr6:62939800-62940200	Weak transcription	H1 Cell Line	embryonic stem cell
21	chr6:62943000-62944000	ZNF genes & repeats	Primary B cells from cord blood	blood
22	chr6:62944000-62988200	Weak transcription	Primary B cells from cord blood	blood
23	chr6:62949200-62949800	ZNF genes & repeats	Fetal Intestine Small	intestine
24	chr6:62949800-62950400	Weak transcription	Fetal Intestine Small	intestine
25	chr6:62952200-62953000	Enhancers	Breast Myoepithelial Primary Cells	Breast
26	chr6:62957400-62957600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
27	chr6:62957400-62957800	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr6:62957400-62958000	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr6:62958000-62958400	Weak transcription	HUES48 Cell Line	embryonic stem cell
30	chr6:62958000-62959400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr6:62958400-62959800	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr6:62958600-62960200	Enhancers	HUES64 Cell Line	embryonic stem cell
33	chr6:62958600-62960800	Enhancers	iPS-20b Cell Line	embryonic stem cell
34	chr6:62959000-62960200	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr6:62959400-62960400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
36	chr6:62960800-62961200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
37	chr6:62961200-62961600	Enhancers	iPS-20b Cell Line	embryonic stem cell
38	chr6:62964200-62964800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr6:62969800-62970200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr6:62970400-62970800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr6:62974200-62974600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr6:62974600-62975000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr6:62974600-62975000	Enhancers	HUES64 Cell Line	embryonic stem cell
44	chr6:62975000-62976400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr6:62975800-62976200	Enhancers	Fetal Intestine Small	intestine
46	chr6:62975800-62976400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
47	chr6:62976000-62977200	Enhancers	Primary B cells from peripheral blood	blood
48	chr6:62976400-62994400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
49	chr6:62988200-62988400	Enhancers	Primary B cells from peripheral blood	blood
50	chr6:62988200-62988800	Enhancers	Primary B cells from cord blood	blood

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