Variant report

Variant	nsv885967
Chromosome Location	chr6:63152724-63605221
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:63600979-63601266	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:63485401-63485684	HepG2	liver:	n/a	n/a
3	BACH1	chr6:63343076-63343099	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr6:63275845-63276042	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr6:63476348-63476567	GM12878	blood:	n/a	n/a
6	BCL11A	chr6:63261207-63261405	GM12878	blood:	n/a	n/a
7	BRCA1	chr6:63297856-63298053	H1-hESC	embryonic stem cell:	n/a	n/a
8	CBX3	chr6:63362679-63362919	K562	blood:	n/a	n/a
9	CBX3	chr6:63362595-63362988	HCT-116	colon:	n/a	n/a
10	CBX3	chr6:63362575-63362854	K562	blood:	n/a	n/a
11	CCNT2	chr6:63244049-63244248	K562	blood:	n/a	n/a
12	CEBPB	chr6:63195691-63195891	A549	lung:	n/a	chr6:63195781-63195792
13	CEBPB	chr6:63184713-63185024	A549	lung:	n/a	chr6:63184880-63184891
14	CEBPB	chr6:63476559-63476780	HepG2	liver:	n/a	chr6:63476688-63476699
15	CEBPB	chr6:63554061-63554290	A549	lung:	n/a	n/a
16	CEBPB	chr6:63316649-63316921	HepG2	liver:	n/a	n/a
17	CEBPB	chr6:63326531-63326747	HepG2	liver:	n/a	chr6:63326660-63326671
18	CEBPB	chr6:63517862-63517964	K562	blood:	n/a	chr6:63517900-63517913 chr6:63517900-63517911
19	CEBPB	chr6:63350334-63350675	HepG2	liver:	n/a	chr6:63350634-63350645 chr6:63350477-63350488 chr6:63350476-63350489
20	CEBPB	chr6:63486528-63486800	HepG2	liver:	n/a	n/a
21	CEBPB	chr6:63520524-63520675	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr6:63184778-63185113	ECC-1	luminal epithelium:	n/a	chr6:63184880-63184891
23	CEBPB	chr6:63512795-63513283	MCF-7	breast:	n/a	chr6:63513016-63513027
24	CEBPB	chr6:63195602-63195944	HepG2	liver:	n/a	chr6:63195781-63195792
25	CEBPB	chr6:63200426-63200489	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr6:63326483-63326806	MCF-7	breast:	n/a	chr6:63326660-63326671
27	CEBPB	chr6:63200359-63200638	HepG2	liver:	n/a	chr6:63200482-63200495 chr6:63200482-63200493 chr6:63200484-63200495 chr6:63200482-63200495 chr6:63200482-63200495 chr6:63200484-63200495
28	CEBPB	chr6:63234202-63234462	HepG2	liver:	n/a	n/a
29	CEBPB	chr6:63184706-63185048	ECC-1	luminal epithelium:	n/a	chr6:63184880-63184891
30	CEBPB	chr6:63326560-63326798	MCF-7	breast:	n/a	chr6:63326660-63326671
31	CEBPB	chr6:63195679-63195883	H1-hESC	embryonic stem cell:	n/a	chr6:63195781-63195792
32	CEBPB	chr6:63184716-63185068	HepG2	liver:	n/a	chr6:63184880-63184891
33	CEBPB	chr6:63571959-63572191	HepG2	liver:	n/a	chr6:63572068-63572079
34	CEBPB	chr6:63350553-63351067	A549	lung:	n/a	chr6:63350634-63350645
35	CEBPB	chr6:63525042-63525285	HepG2	liver:	n/a	chr6:63525158-63525169
36	CEBPB	chr6:63189520-63189747	A549	lung:	n/a	chr6:63189603-63189614 chr6:63189604-63189615 chr6:63189602-63189619 chr6:63189603-63189616
37	CEBPB	chr6:63186918-63187244	HepG2	liver:	n/a	chr6:63187071-63187082
38	CEBPB	chr6:63512957-63513198	IMR90	lung:	n/a	chr6:63513016-63513027
39	CEBPB	chr6:63195619-63195937	IMR90	lung:	n/a	chr6:63195781-63195792
40	CEBPB	chr6:63512982-63513172	H1-hESC	embryonic stem cell:	n/a	chr6:63513016-63513027
41	CEBPB	chr6:63189473-63189777	HepG2	liver:	n/a	chr6:63189603-63189614 chr6:63189604-63189615 chr6:63189602-63189619 chr6:63189603-63189616
42	CEBPB	chr6:63541693-63541860	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr6:63216022-63216260	HepG2	liver:	n/a	chr6:63216135-63216146 chr6:63216135-63216148 chr6:63216132-63216149
44	CEBPB	chr6:63209671-63210000	HepG2	liver:	n/a	chr6:63209812-63209823
45	CEBPB	chr6:63165587-63165869	IMR90	lung:	n/a	n/a
46	CEBPB	chr6:63517820-63517987	HepG2	liver:	n/a	chr6:63517900-63517913 chr6:63517900-63517911
47	CEBPB	chr6:63184708-63185066	IMR90	lung:	n/a	chr6:63184880-63184891
48	CEBPB	chr6:63377486-63377807	HepG2	liver:	n/a	chr6:63377653-63377664
49	CEBPB	chr6:63311156-63311399	A549	lung:	n/a	n/a
50	CEBPB	chr6:63512841-63513198	HepG2	liver:	n/a	chr6:63513016-63513027

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:63553575-63553625	NB4	blood:	n/a
2	chr6:63553575-63553625	NB4	blood:	n/a
3	chr6:63572411-63572461	CMK	blood:	n/a
4	chr6:63572411-63572461	AG10803	skin:	n/a
5	chr6:63226373-63226423	GM12892	blood:	n/a
6	chr6:63553575-63553625	IMR90	lung:	fetal
7	chr6:63553575-63553625	AG09309	skin:	n/a
8	chr6:63572411-63572461	SKMC	muscle:	n/a
9	chr6:63226373-63226423	T-47D	breast:	n/a
10	chr6:63572411-63572461	ovcar-3	ovarian:	n/a
11	chr6:63226373-63226423	BE2_C	brain:	n/a
12	chr6:63553575-63553625	MCF10A-Er-Src	breast:	n/a
13	chr6:63553696-63553746	HEK293	kidney:	embryo
14	chr6:63553575-63553625	HNPCEpiC	eye:	n/a
15	chr6:63157784-63157834	SKMC	muscle:	n/a
16	chr6:63553696-63553746	CMK	blood:	n/a
17	chr6:63226373-63226423	ProgFib	skin:	n/a
18	chr6:63572411-63572461	HIPEpiC	eye:	n/a
19	chr6:63157784-63157834	Caco-2	colon:	n/a
20	chr6:63226373-63226423	HEK293	kidney:	embryo
21	chr6:63226373-63226423	NHBE	bronchial:	n/a
22	chr6:63157784-63157834	AG04450	lung:	fetal
23	chr6:63226373-63226423	NT2-D1	testis:	n/a
24	chr6:63553575-63553625	AG04449	skin:	fetal
25	chr6:63572411-63572461	HRPEpiC	eye:	n/a
26	chr6:63553696-63553746	ovcar-3	ovarian:	n/a
27	chr6:63157784-63157834	GM12878	blood:	n/a
28	chr6:63226373-63226423	ECC-1	luminal epithelium:	n/a
29	chr6:63553575-63553625	RPTEC	kidney:	n/a
30	chr6:63553696-63553746	HCPEpiC	choroid plexus:	n/a
31	chr6:63553575-63553625	A549	lung:	n/a
32	chr6:63553575-63553625	HMEC	breast:	n/a
33	chr6:63157784-63157834	BE2_C	brain:	n/a
34	chr6:63572411-63572461	AG09319	gingival:	n/a
35	chr6:63572411-63572461	NH-A	brain:	n/a
36	chr6:63226373-63226423	AG04450	lung:	fetal
37	chr6:63572411-63572461	Jurkat	blood:	n/a
38	chr6:63226373-63226423	GM12878	blood:	n/a
39	chr6:63553575-63553625	NT2-D1	testis:	n/a
40	chr6:63226373-63226423	ovcar-3	ovarian:	n/a
41	chr6:63553575-63553625	GM12878	blood:	n/a
42	chr6:63157784-63157834	HPAEpiC	pulmonary alveolar:	n/a
43	chr6:63572411-63572461	NB4	blood:	n/a
44	chr6:63572411-63572461	HCM	heart:	n/a
45	chr6:63226373-63226423	Hela-S3	cervix:	n/a
46	chr6:63157784-63157834	HUVEC	blood vessel:	n/a
47	chr6:63572411-63572461	U87	brain:	n/a
48	chr6:63553575-63553625	HAEpiC	amniotic membrane:	n/a
49	chr6:63553575-63553625	GM12892	blood:	n/a
50	chr6:63226373-63226423	LNCaP	prostate:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:28560124..28560625-chr6:63259614..63260114,2	NB4	blood:
2	chr6:63278592..63281366-chr6:63283322..63285509,2	MCF-7	breast:
3	chr6:63514284..63517012-chr6:63519494..63521413,2	MCF-7	breast:
4	chr6:63211094..63213340-chr6:63214100..63215970,2	MCF-7	breast:
5	chr6:63601380..63602369-chr6:63983063..63983726,2	MCF-7	breast:
6	chr6:63381016..63382588-chr6:63383396..63385763,2	K562	blood:
7	chr6:63441335..63443879-chr6:63445998..63448155,2	K562	blood:
8	chr17:41400213..41402082-chr6:63530273..63531773,2	MCF-7	breast:
9	chr6:63381016..63382588-chr6:63383396..63385763,2	K562	blood:
10	chr17:41400161..41402651-chr6:63528753..63531753,3	K562	blood:
11	chr1:17229945..17231648-chr6:63349079..63350580,2	MCF-7	breast:
12	chr17:41400811..41402656-chr6:63530253..63531773,2	MCF-7	breast:
13	chr17:41466229..41468054-chr6:63528754..63531753,2	K562	blood:
14	chr6:63514284..63517012-chr6:63519494..63521413,2	MCF-7	breast:
15	chr6:62518549..62519303-chr6:63600674..63601315,2	MCF-7	breast:
16	chr17:41465690..41468054-chr6:63528753..63530254,3	MCF-7	breast:
17	chr6:63278592..63281366-chr6:63283322..63285509,2	MCF-7	breast:
18	chr6:63441335..63443879-chr6:63445998..63448155,2	K562	blood:
19	chr17:41466567..41467237-chr6:63529754..63530273,2	NB4	blood:
20	chr22:19006105..19008372-chr6:63457723..63459244,2	K562	blood:
21	chr6:63211094..63213340-chr6:63214100..63215970,2	MCF-7	breast:
22	chr17:41399298..41401661-chr6:63530253..63531773,2	K562	blood:

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

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

Extended variants
information (count: 11910 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:11910 , 50 per page) page: 1 2 3 4 5 6 7 ... 239

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs646854	chr6:63152724-63152725	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs549608352	chr6:63152750-63152751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs571361631	chr6:63152768-63152769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs531998320	chr6:63152775-63152776	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs542855259	chr6:63152795-63152796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs561204608	chr6:63152823-63152824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs146031573	chr6:63152837-63152838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs112662438	chr6:63152892-63152893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs528782792	chr6:63152984-63152985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs113370010	chr6:63152998-63152999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs139966447	chr6:63153059-63153060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs186313396	chr6:63153066-63153067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs554757783	chr6:63153075-63153076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs141174903	chr6:63153088-63153089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs58958975	chr6:63153093-63153094	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs556364467	chr6:63153096-63153097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs578067548	chr6:63153105-63153106	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs190386394	chr6:63153109-63153110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs675437	chr6:63153118-63153119	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs572365441	chr6:63153133-63153134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs561954406	chr6:63153185-63153186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs182980196	chr6:63153196-63153197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs186944662	chr6:63153198-63153199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs576223325	chr6:63153267-63153268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs659539	chr6:63153277-63153278	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs564809252	chr6:63153309-63153310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs58786068	chr6:63153311-63153312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs372543705	chr6:63153320-63153321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs552770299	chr6:63153350-63153351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs191581480	chr6:63153389-63153390	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs547035385	chr6:63153453-63153454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs182565025	chr6:63153459-63153460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs150713083	chr6:63153511-63153512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs373957710	chr6:63153536-63153537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs78137265	chr6:63153582-63153583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs570000785	chr6:63153633-63153634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs551503429	chr6:63153697-63153698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs187693643	chr6:63153829-63153830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs552369125	chr6:63153854-63153855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs581435	chr6:63153926-63153927	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs370514873	chr6:63153928-63153929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs530693314	chr6:63153951-63153952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs10455725	chr6:63153955-63153956	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs553834661	chr6:63153984-63153985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs567537464	chr6:63154034-63154035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs534942393	chr6:63154044-63154045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs192360211	chr6:63154067-63154068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs554829896	chr6:63154112-63154113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs576359692	chr6:63154145-63154146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs543628611	chr6:63154180-63154181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

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
Acute lymphoblastic leukemia	18458336	CNVD
Schizophrenia	23813976	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	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
Developmental delay	21147756	CNVD

Chromatin state (count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:63151400-63155400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr6:63155400-63155800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr6:63155400-63155800	ZNF genes & repeats	Pancreas	Pancrea
4	chr6:63156400-63157000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr6:63156600-63157200	Enhancers	Primary B cells from peripheral blood	blood
6	chr6:63156600-63157800	Enhancers	Primary B cells from cord blood	blood
7	chr6:63157000-63158000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr6:63157200-63158000	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr6:63157600-63158000	Enhancers	H9 Cell Line	embryonic stem cell
10	chr6:63157600-63158000	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr6:63157600-63158000	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr6:63157600-63158200	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr6:63166200-63166600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr6:63174400-63175800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr6:63174800-63175600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr6:63187800-63188400	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr6:63188200-63188400	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr6:63188400-63188600	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr6:63188400-63189400	Weak transcription	HUES6 Cell Line	embryonic stem cell
20	chr6:63188400-63189400	Weak transcription	HUES64 Cell Line	embryonic stem cell
21	chr6:63188600-63189600	Weak transcription	HUES48 Cell Line	embryonic stem cell
22	chr6:63189400-63190200	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr6:63189400-63190400	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr6:63189600-63190000	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr6:63189600-63190000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr6:63189600-63190200	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chr6:63189800-63190200	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr6:63190000-63190400	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr6:63190200-63190400	Enhancers	Fetal Intestine Small	intestine
30	chr6:63190400-63191800	Weak transcription	Fetal Intestine Small	intestine
31	chr6:63191800-63193000	Enhancers	Fetal Intestine Small	intestine
32	chr6:63201200-63201400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr6:63202200-63202600	Active TSS	HepG2	liver
34	chr6:63210600-63217400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr6:63217400-63217600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr6:63220200-63220400	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr6:63220600-63225000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
38	chr6:63222800-63223200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr6:63223200-63224400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr6:63224400-63224800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr6:63224600-63224800	Enhancers	Cortex derived primary cultured neurospheres	brain
42	chr6:63224600-63225000	Enhancers	iPS-15b Cell Line	embryonic stem cell
43	chr6:63224600-63226400	Enhancers	HUES64 Cell Line	embryonic stem cell
44	chr6:63224800-63225800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr6:63224800-63225800	Weak transcription	Cortex derived primary cultured neurospheres	brain
46	chr6:63225000-63225400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
47	chr6:63225000-63226000	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr6:63225200-63225800	Enhancers	iPS-20b Cell Line	embryonic stem cell
49	chr6:63225400-63226200	Enhancers	HUES48 Cell Line	embryonic stem cell
50	chr6:63225400-63226800	Enhancers	iPS-15b Cell Line	embryonic stem cell

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