Variant report

Variant	nsv532025
Chromosome Location	chr6:62944349-63571677
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1465)
CpG islands
(count:1221)
Chromatin interactive
region (count:22)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1465 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:63485401-63485684	HepG2	liver:	n/a	n/a
2	ATF2	chr6:63077568-63077881	GM12878	blood:	n/a	n/a
3	ATF2	chr6:63008561-63009076	GM12878	blood:	n/a	n/a
4	ATF2	chr6:63008621-63009133	GM12878	blood:	n/a	n/a
5	BACH1	chr6:63275845-63276042	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr6:63036580-63036810	H1-hESC	embryonic stem cell:	n/a	chr6:63036749-63036763
7	BACH1	chr6:62996403-62996585	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr6:63343076-63343099	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr6:62964878-62964884	K562	blood:	n/a	n/a
10	BACH1	chr6:62995853-62996194	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr6:63476348-63476567	GM12878	blood:	n/a	n/a
12	BCL11A	chr6:63008564-63009026	GM12878	blood:	n/a	n/a
13	BCL11A	chr6:63261207-63261405	GM12878	blood:	n/a	n/a
14	BCL3	chr6:63008674-63008913	GM12878	blood:	n/a	n/a
15	BCLAF1	chr6:63008581-63009054	GM12878	blood:	n/a	n/a
16	BHLHE40	chr6:63115576-63115579	GM12878	blood:	n/a	n/a
17	BHLHE40	chr6:63008716-63009043	GM12878	blood:	n/a	n/a
18	BRCA1	chr6:63297856-63298053	H1-hESC	embryonic stem cell:	n/a	n/a
19	CBX3	chr6:63362679-63362919	K562	blood:	n/a	n/a
20	CBX3	chr6:63362575-63362854	K562	blood:	n/a	n/a
21	CBX3	chr6:63362595-63362988	HCT-116	colon:	n/a	n/a
22	CCNT2	chr6:63244049-63244248	K562	blood:	n/a	n/a
23	CEBPB	chr6:63184725-63185043	Hela-S3	cervix:	n/a	chr6:63184880-63184891
24	CEBPB	chr6:63350553-63351067	A549	lung:	n/a	chr6:63350634-63350645
25	CEBPB	chr6:63512957-63513198	IMR90	lung:	n/a	chr6:63513016-63513027
26	CEBPB	chr6:63195679-63195883	H1-hESC	embryonic stem cell:	n/a	chr6:63195781-63195792
27	CEBPB	chr6:63165587-63165869	IMR90	lung:	n/a	n/a
28	CEBPB	chr6:62944204-62944407	HepG2	liver:	n/a	chr6:62944258-62944269
29	CEBPB	chr6:62946881-62947231	A549	lung:	n/a	chr6:62947127-62947138
30	CEBPB	chr6:63541693-63541860	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr6:63377486-63377807	HepG2	liver:	n/a	chr6:63377653-63377664
32	CEBPB	chr6:63189473-63189777	HepG2	liver:	n/a	chr6:63189603-63189614 chr6:63189604-63189615 chr6:63189602-63189619 chr6:63189603-63189616
33	CEBPB	chr6:62946841-62947210	HepG2	liver:	n/a	chr6:62947127-62947138
34	CEBPB	chr6:63184719-63185081	H1-hESC	embryonic stem cell:	n/a	chr6:63184880-63184891
35	CEBPB	chr6:63234202-63234462	HepG2	liver:	n/a	n/a
36	CEBPB	chr6:63512795-63513283	MCF-7	breast:	n/a	chr6:63513016-63513027
37	CEBPB	chr6:63512982-63513172	H1-hESC	embryonic stem cell:	n/a	chr6:63513016-63513027
38	CEBPB	chr6:63520524-63520675	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr6:63209671-63210000	HepG2	liver:	n/a	chr6:63209812-63209823
40	CEBPB	chr6:63184713-63185024	A549	lung:	n/a	chr6:63184880-63184891
41	CEBPB	chr6:63216022-63216260	HepG2	liver:	n/a	chr6:63216135-63216146 chr6:63216135-63216148 chr6:63216132-63216149
42	CEBPB	chr6:63135857-63136005	K562	blood:	n/a	chr6:63135923-63135932 chr6:63135921-63135934 chr6:63135923-63135932 chr6:63135923-63135932 chr6:63135923-63135932 chr6:63135923-63135934
43	CEBPB	chr6:63184708-63185066	IMR90	lung:	n/a	chr6:63184880-63184891
44	CEBPB	chr6:63184716-63185068	HepG2	liver:	n/a	chr6:63184880-63184891
45	CEBPB	chr6:63189520-63189747	A549	lung:	n/a	chr6:63189603-63189614 chr6:63189604-63189615 chr6:63189602-63189619 chr6:63189603-63189616
46	CEBPB	chr6:63517862-63517964	K562	blood:	n/a	chr6:63517900-63517913 chr6:63517900-63517911
47	CEBPB	chr6:63195602-63195944	HepG2	liver:	n/a	chr6:63195781-63195792
48	CEBPB	chr6:63186918-63187244	HepG2	liver:	n/a	chr6:63187071-63187082
49	CEBPB	chr6:63326560-63326798	MCF-7	breast:	n/a	chr6:63326660-63326671
50	CEBPB	chr6:63072299-63072645	HepG2	liver:	n/a	chr6:63072437-63072450 chr6:63072437-63072450 chr6:63072438-63072449 chr6:63072628-63072641

(count:1221 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:63553696-63553746	U87	brain:	n/a
2	chr6:63553696-63553746	U87	brain:	n/a
3	chr6:62996119-62996169	ProgFib	skin:	n/a
4	chr6:62996132-62996182	GM12892	blood:	n/a
5	chr6:63553575-63553625	HRE	kidney:	n/a
6	chr6:62995523-62995573	H1-hESC	embryonic stem cell:	embryo
7	chr6:62995523-62995573	HRCEpiC	kidney:	n/a
8	chr6:62996299-62996349	PFSK-1	brain:	n/a
9	chr6:62996132-62996182	SK-N-MC	brain:	n/a
10	chr6:62995876-62995926	HAEpiC	amniotic membrane:	n/a
11	chr6:62996627-62996677	AG10803	skin:	n/a
12	chr6:63157784-63157834	BJ	skin:	n/a
13	chr6:62996664-62996714	HRCEpiC	kidney:	n/a
14	chr6:62996119-62996169	HL-60	blood:	n/a
15	chr6:62996214-62996264	SK-N-SH_RA	brain:	n/a
16	chr6:62996627-62996677	U87	brain:	n/a
17	chr6:63157784-63157834	MCF-7	breast:	n/a
18	chr6:62996119-62996169	NT2-D1	testis:	n/a
19	chr6:62995963-62996013	GM06990	blood:	n/a
20	chr6:62976042-62976092	PrEC	prostate:	n/a
21	chr6:62995876-62995926	NT2-D1	testis:	n/a
22	chr6:62996664-62996714	GM12878	blood:	n/a
23	chr6:63038652-63038702	BJ	skin:	n/a
24	chr6:62995876-62995926	NHBE	bronchial:	n/a
25	chr6:62996627-62996677	HCPEpiC	choroid plexus:	n/a
26	chr6:62996119-62996169	HRPEpiC	eye:	n/a
27	chr6:62996627-62996677	GM19239	blood:	n/a
28	chr6:62996119-62996169	AG10803	skin:	n/a
29	chr6:62996183-62996233	HIPEpiC	eye:	n/a
30	chr6:62996697-62996747	K562	blood:	n/a
31	chr6:62996022-62996072	HNPCEpiC	eye:	n/a
32	chr6:62996022-62996072	HCF	heart:	n/a
33	chr6:62976042-62976092	A549	lung:	n/a
34	chr6:63553696-63553746	NT2-D1	testis:	n/a
35	chr6:63038652-63038702	HIPEpiC	eye:	n/a
36	chr6:62996130-62996180	SK-N-MC	brain:	n/a
37	chr6:62996627-62996677	HRPEpiC	eye:	n/a
38	chr6:62995523-62995573	NH-A	brain:	n/a
39	chr6:62996627-62996677	A549	lung:	n/a
40	chr6:62995876-62995926	GM19239	blood:	n/a
41	chr6:62996132-62996182	SKMC	muscle:	n/a
42	chr6:62996627-62996677	HCF	heart:	n/a
43	chr6:62996664-62996714	NB4	blood:	n/a
44	chr6:62995876-62995926	ovcar-3	ovarian:	n/a
45	chr6:62996132-62996182	NB4	blood:	n/a
46	chr6:63226373-63226423	ProgFib	skin:	n/a
47	chr6:63157784-63157834	NHBE	bronchial:	n/a
48	chr6:62996214-62996264	BE2_C	brain:	n/a
49	chr6:63038652-63038702	BE2_C	brain:	n/a
50	chr6:62996130-62996180	GM19239	blood:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:63211094..63213340-chr6:63214100..63215970,2	MCF-7	breast:
2	chr17:41400161..41402651-chr6:63528753..63531753,3	K562	blood:
3	chr6:63381016..63382588-chr6:63383396..63385763,2	K562	blood:
4	chr17:41399298..41401661-chr6:63530253..63531773,2	K562	blood:
5	chr6:63441335..63443879-chr6:63445998..63448155,2	K562	blood:
6	chr17:41465690..41468054-chr6:63528753..63530254,3	MCF-7	breast:
7	chr17:41400811..41402656-chr6:63530253..63531773,2	MCF-7	breast:
8	chr1:28560124..28560625-chr6:63259614..63260114,2	NB4	blood:
9	chr17:41400213..41402082-chr6:63530273..63531773,2	MCF-7	breast:
10	chr17:41466567..41467237-chr6:63529754..63530273,2	NB4	blood:
11	chr6:63278592..63281366-chr6:63283322..63285509,2	MCF-7	breast:
12	chr22:19006105..19008372-chr6:63457723..63459244,2	K562	blood:
13	chr6:63381016..63382588-chr6:63383396..63385763,2	K562	blood:
14	chr6:63211094..63213340-chr6:63214100..63215970,2	MCF-7	breast:
15	chr6:62973850..62974714-chr7:113350282..113350966,2	MCF-7	breast:
16	chr6:62518763..62519292-chr6:62993656..62994388,2	MCF-7	breast:
17	chr6:63514284..63517012-chr6:63519494..63521413,2	MCF-7	breast:
18	chr1:17229945..17231648-chr6:63349079..63350580,2	MCF-7	breast:
19	chr17:41466229..41468054-chr6:63528754..63531753,2	K562	blood:
20	chr6:63441335..63443879-chr6:63445998..63448155,2	K562	blood:
21	chr6:63278592..63281366-chr6:63283322..63285509,2	MCF-7	breast:
22	chr6:63514284..63517012-chr6:63519494..63521413,2	MCF-7	breast:

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

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

No data

Variant related genes	Relation type
ENSG00000264410	TF binding region
ENSG00000216072	TF binding region
KHDRBS2	TF binding region
ENSG00000217067	TF binding region
ENSG00000216859	TF binding region
ENSG00000262566	TF binding region
ENSG00000264410	CpG island
ENSG00000216072	CpG island
KHDRBS2	CpG island
ENSG00000217067	CpG island
ENSG00000216859	CpG island
ENSG00000262566	CpG island
ENSG00000270393	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000272426	chromatin interactions

Extended variants
information (count: 14141 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:14141 , 50 per page) page: 1 2 3 4 5 6 7 ... 283

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs559055594	chr6:62944356-62944357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs576239340	chr6:62944382-62944383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs530474028	chr6:62944385-62944386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs531930301	chr6:62944410-62944411	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs369404818	chr6:62944436-62944437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs564575581	chr6:62944457-62944458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs532114155	chr6:62944526-62944527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs540072731	chr6:62944540-62944541	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs149516462	chr6:62944584-62944585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs191041299	chr6:62944594-62944595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs143991214	chr6:62944608-62944609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs148693489	chr6:62944721-62944722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs569860652	chr6:62944745-62944746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs537383319	chr6:62944819-62944820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs558875325	chr6:62944842-62944843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs577980958	chr6:62944888-62944889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs573472362	chr6:62944896-62944897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs539044689	chr6:62944905-62944906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs553840725	chr6:62944913-62944914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs182874971	chr6:62944949-62944950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs542710941	chr6:62944974-62944975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs10570985	chr6:62944976-62944977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs111385859	chr6:62945007-62945008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs561188210	chr6:62945036-62945037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs187554660	chr6:62945043-62945044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs200242779	chr6:62945060-62945061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs543737010	chr6:62945092-62945093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs142215766	chr6:62945101-62945102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs532662883	chr6:62945108-62945109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs116322565	chr6:62945111-62945112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs190169739	chr6:62945133-62945134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs6934817	chr6:62945142-62945143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs183418950	chr6:62945162-62945163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs187572413	chr6:62945184-62945185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs537219876	chr6:62945204-62945205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs76680312	chr6:62945236-62945237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs551083956	chr6:62945255-62945256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs151155661	chr6:62945259-62945260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs192813305	chr6:62945278-62945279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs554186630	chr6:62945289-62945290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs565927299	chr6:62945334-62945335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs536383914	chr6:62945356-62945357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs554623522	chr6:62945407-62945408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs184368258	chr6:62945426-62945427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs139431651	chr6:62945434-62945435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs558841330	chr6:62945456-62945457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs546261505	chr6:62945484-62945485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs187571740	chr6:62945498-62945499	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs192565498	chr6:62945513-62945514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs184241799	chr6:62945593-62945594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

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
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
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	20164920	CNVD
Prostate cancer	16573809	CNVD
Ovarian cancer	19835627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Glioblastoma multiforme	22286061	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16272173	CNVD

Chromatin state (count:877 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:62944000-62988200	Weak transcription	Primary B cells from cord blood	blood
2	chr6:62949200-62949800	ZNF genes & repeats	Fetal Intestine Small	intestine
3	chr6:62949800-62950400	Weak transcription	Fetal Intestine Small	intestine
4	chr6:62952200-62953000	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr6:62957400-62957600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr6:62957400-62957800	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr6:62957400-62958000	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr6:62958000-62958400	Weak transcription	HUES48 Cell Line	embryonic stem cell
9	chr6:62958000-62959400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr6:62958400-62959800	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr6:62958600-62960200	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr6:62958600-62960800	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr6:62959000-62960200	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr6:62959400-62960400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
15	chr6:62960800-62961200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
16	chr6:62961200-62961600	Enhancers	iPS-20b Cell Line	embryonic stem cell
17	chr6:62964200-62964800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr6:62969800-62970200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr6:62970400-62970800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr6:62974200-62974600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr6:62974600-62975000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr6:62974600-62975000	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chr6:62975000-62976400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr6:62975800-62976200	Enhancers	Fetal Intestine Small	intestine
25	chr6:62975800-62976400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr6:62976000-62977200	Enhancers	Primary B cells from peripheral blood	blood
27	chr6:62976400-62994400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr6:62988200-62988400	Enhancers	Primary B cells from peripheral blood	blood
29	chr6:62988200-62988800	Enhancers	Primary B cells from cord blood	blood
30	chr6:62988400-62989800	Weak transcription	Primary B cells from peripheral blood	blood
31	chr6:62988800-62993200	Weak transcription	Primary B cells from cord blood	blood
32	chr6:62989600-62990000	Enhancers	ES-I3 Cell Line	embryonic stem cell
33	chr6:62989600-62990000	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr6:62989600-62990400	Enhancers	H1 Cell Line	embryonic stem cell
35	chr6:62989800-62990400	Enhancers	Primary B cells from peripheral blood	blood
36	chr6:62990000-62991800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr6:62990000-62993600	Weak transcription	HUES64 Cell Line	embryonic stem cell
38	chr6:62990400-62993400	Weak transcription	Primary B cells from peripheral blood	blood
39	chr6:62990400-62994000	Weak transcription	H1 Cell Line	embryonic stem cell
40	chr6:62990800-62991000	Enhancers	Fetal Brain Female	brain
41	chr6:62991200-62992400	Weak transcription	Fetal Brain Female	brain
42	chr6:62991800-62996800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr6:62992400-62992600	Enhancers	Fetal Brain Female	brain
44	chr6:62992600-62993000	Enhancers	Fetal Intestine Small	intestine
45	chr6:62992600-62993200	Enhancers	Fetal Intestine Large	intestine
46	chr6:62992600-62994800	Active TSS	Fetal Brain Female	brain
47	chr6:62992600-62997000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
48	chr6:62992800-62994800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr6:62992800-62997000	Active TSS	Brain Angular Gyrus	brain
50	chr6:62992800-62997000	Active TSS	Brain Inferior Temporal Lobe	brain

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