Variant report

Variant	nsv885968
Chromosome Location	chr6:63199731-63585140
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:799)
CpG islands
(count:244)
Chromatin interactive
region (count:20)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:799 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

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	BACH1	chr6:63275845-63276042	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr6:63343076-63343099	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr6:63476348-63476567	GM12878	blood:	n/a	n/a
5	BCL11A	chr6:63261207-63261405	GM12878	blood:	n/a	n/a
6	BRCA1	chr6:63297856-63298053	H1-hESC	embryonic stem cell:	n/a	n/a
7	CBX3	chr6:63362595-63362988	HCT-116	colon:	n/a	n/a
8	CBX3	chr6:63362679-63362919	K562	blood:	n/a	n/a
9	CBX3	chr6:63362575-63362854	K562	blood:	n/a	n/a
10	CCNT2	chr6:63244049-63244248	K562	blood:	n/a	n/a
11	CEBPB	chr6:63311156-63311399	A549	lung:	n/a	n/a
12	CEBPB	chr6:63525042-63525285	HepG2	liver:	n/a	chr6:63525158-63525169
13	CEBPB	chr6:63316649-63316921	HepG2	liver:	n/a	n/a
14	CEBPB	chr6:63554061-63554290	A549	lung:	n/a	n/a
15	CEBPB	chr6:63311181-63311407	MCF-7	breast:	n/a	n/a
16	CEBPB	chr6:63479626-63479944	HepG2	liver:	n/a	chr6:63479783-63479794
17	CEBPB	chr6:63512957-63513198	IMR90	lung:	n/a	chr6:63513016-63513027
18	CEBPB	chr6:63512795-63513283	MCF-7	breast:	n/a	chr6:63513016-63513027
19	CEBPB	chr6:63200426-63200489	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr6:63234202-63234462	HepG2	liver:	n/a	n/a
21	CEBPB	chr6:63350553-63351067	A549	lung:	n/a	chr6:63350634-63350645
22	CEBPB	chr6:63326531-63326747	HepG2	liver:	n/a	chr6:63326660-63326671
23	CEBPB	chr6:63517862-63517964	K562	blood:	n/a	chr6:63517900-63517913 chr6:63517900-63517911
24	CEBPB	chr6:63350334-63350675	HepG2	liver:	n/a	chr6:63350634-63350645 chr6:63350477-63350488 chr6:63350476-63350489
25	CEBPB	chr6:63377486-63377807	HepG2	liver:	n/a	chr6:63377653-63377664
26	CEBPB	chr6:63517820-63517987	HepG2	liver:	n/a	chr6:63517900-63517913 chr6:63517900-63517911
27	CEBPB	chr6:63326483-63326806	MCF-7	breast:	n/a	chr6:63326660-63326671
28	CEBPB	chr6:63512841-63513198	HepG2	liver:	n/a	chr6:63513016-63513027
29	CEBPB	chr6:63476559-63476780	HepG2	liver:	n/a	chr6:63476688-63476699
30	CEBPB	chr6:63486528-63486800	HepG2	liver:	n/a	n/a
31	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
32	CEBPB	chr6:63512982-63513172	H1-hESC	embryonic stem cell:	n/a	chr6:63513016-63513027
33	CEBPB	chr6:63326560-63326798	MCF-7	breast:	n/a	chr6:63326660-63326671
34	CEBPB	chr6:63209671-63210000	HepG2	liver:	n/a	chr6:63209812-63209823
35	CEBPB	chr6:63571959-63572191	HepG2	liver:	n/a	chr6:63572068-63572079
36	CEBPB	chr6:63216022-63216260	HepG2	liver:	n/a	chr6:63216135-63216146 chr6:63216135-63216148 chr6:63216132-63216149
37	CEBPB	chr6:63520524-63520675	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr6:63541693-63541860	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPZ	chr6:63362626-63362905	HepG2	liver:	n/a	n/a
40	CHD1	chr6:63347777-63347984	H1-hESC	embryonic stem cell:	n/a	n/a
41	CHD1	chr6:63297860-63298054	H1-hESC	embryonic stem cell:	n/a	n/a
42	CHD2	chr6:63576492-63576565	GM12878	blood:	n/a	n/a
43	CHD2	chr6:63457023-63457040	GM12878	blood:	n/a	n/a
44	CREB1	chr6:63226203-63226525	H1-hESC	embryonic stem cell:	n/a	n/a
45	CREB1	chr6:63226126-63226653	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr6:63485306-63485911	HepG2	liver:	n/a	chr6:63485525-63485541 chr6:63485526-63485539 chr6:63485524-63485542 chr6:63485519-63485540 chr6:63485530-63485539
47	CTCF	chr6:63485723-63485875	GM10248	blood:	n/a	n/a
48	CTCF	chr6:63485420-63485570	HRE	kidney:	n/a	chr6:63485525-63485541 chr6:63485526-63485539 chr6:63485524-63485542 chr6:63485519-63485540 chr6:63485530-63485539
49	CTCF	chr6:63324480-63324630	HEK293	kidney:	n/a	n/a
50	CTCF	chr6:63485267-63486123	A549	lung:	n/a	chr6:63485525-63485541 chr6:63485526-63485539 chr6:63485524-63485542 chr6:63485519-63485540 chr6:63485530-63485539

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:63553575-63553625	ProgFib	skin:	n/a
2	chr6:63226373-63226423	HCM	heart:	n/a
3	chr6:63553575-63553625	GM19239	blood:	n/a
4	chr6:63553696-63553746	AG09309	skin:	n/a
5	chr6:63572411-63572461	Caco-2	colon:	n/a
6	chr6:63553575-63553625	CMK	blood:	n/a
7	chr6:63553696-63553746	ovcar-3	ovarian:	n/a
8	chr6:63553575-63553625	PrEC	prostate:	n/a
9	chr6:63553696-63553746	RPTEC	kidney:	n/a
10	chr6:63553696-63553746	HepG2	liver:	n/a
11	chr6:63572411-63572461	NH-A	brain:	n/a
12	chr6:63553696-63553746	Jurkat	blood:	n/a
13	chr6:63553575-63553625	BJ	skin:	n/a
14	chr6:63226373-63226423	NT2-D1	testis:	n/a
15	chr6:63226373-63226423	SK-N-SH_RA	brain:	n/a
16	chr6:63553575-63553625	AG04449	skin:	fetal
17	chr6:63226373-63226423	T-47D	breast:	n/a
18	chr6:63226373-63226423	Hela-S3	cervix:	n/a
19	chr6:63226373-63226423	GM06990	blood:	n/a
20	chr6:63553575-63553625	HL-60	blood:	n/a
21	chr6:63572411-63572461	GM19239	blood:	n/a
22	chr6:63553696-63553746	U87	brain:	n/a
23	chr6:63553575-63553625	NT2-D1	testis:	n/a
24	chr6:63553575-63553625	HCF	heart:	n/a
25	chr6:63572411-63572461	HAEpiC	amniotic membrane:	n/a
26	chr6:63226373-63226423	HEEpiC	esophagus:	n/a
27	chr6:63226373-63226423	HepG2	liver:	n/a
28	chr6:63553575-63553625	RPTEC	kidney:	n/a
29	chr6:63553575-63553625	HRCEpiC	kidney:	n/a
30	chr6:63553575-63553625	Jurkat	blood:	n/a
31	chr6:63226373-63226423	ProgFib	skin:	n/a
32	chr6:63572411-63572461	BJ	skin:	n/a
33	chr6:63572411-63572461	AG04450	lung:	fetal
34	chr6:63226373-63226423	AoSMC	blood vessel:	n/a
35	chr6:63226373-63226423	NHDF-neo	bronchial:	n/a
36	chr6:63226373-63226423	K562	blood:	n/a
37	chr6:63226373-63226423	LNCaP	prostate:	n/a
38	chr6:63553696-63553746	K562	blood:	n/a
39	chr6:63553696-63553746	CMK	blood:	n/a
40	chr6:63553575-63553625	AG04450	lung:	fetal
41	chr6:63572411-63572461	U87	brain:	n/a
42	chr6:63572411-63572461	HCF	heart:	n/a
43	chr6:63572411-63572461	CMK	blood:	n/a
44	chr6:63553575-63553625	HEEpiC	esophagus:	n/a
45	chr6:63553575-63553625	PFSK-1	brain:	n/a
46	chr6:63572411-63572461	HL-60	blood:	n/a
47	chr6:63553696-63553746	PFSK-1	brain:	n/a
48	chr6:63553575-63553625	HEK293	kidney:	embryo
49	chr6:63553575-63553625	LNCaP	prostate:	n/a
50	chr6:63553696-63553746	HCT-116	colon:	n/a

(count:20 , 50 per page) page: 1

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

(count:4 , 50 per page) page: 1

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	chr6:63257927-63258177	NONHSAT113334
4	lnc-FKBP1C-2	chr6:63257332-63257472	NONHSAT113334

No data

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

Extended variants
information (count: 10338 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:10338 , 50 per page) page: 1 2 3 4 5 6 7 ... 207

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs57294723	chr6:63201204-63201205	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs146904988	chr6:63201249-63201250	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs181676504	chr6:63201290-63201291	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs536584067	chr6:63201301-63201302	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs184089369	chr6:63201307-63201308	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs573069080	chr6:63201312-63201313	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs556200752	chr6:63201336-63201337	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs188822485	chr6:63201339-63201340	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs576259428	chr6:63201395-63201396	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs187046976	chr6:63202224-63202225	Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs538170565	chr6:63202236-63202237	Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs556308891	chr6:63202239-63202240	Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs373521146	chr6:63202245-63202246	Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs114934151	chr6:63202248-63202249	Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs557978472	chr6:63202252-63202253	Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs6923027	chr6:63202289-63202290	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs540227134	chr6:63202310-63202311	Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs62416859	chr6:63202318-63202319	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs529526540	chr6:63202337-63202338	Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs538943307	chr6:63202343-63202344	Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs557062839	chr6:63202344-63202345	Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs528627818	chr6:63202345-63202346	Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs533367727	chr6:63202361-63202362	Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs551417661	chr6:63202373-63202374	Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs368027721	chr6:63202403-63202404	Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs548689157	chr6:63202450-63202451	Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs566566440	chr6:63202464-63202465	Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs527430168	chr6:63202472-63202473	Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs189921964	chr6:63202473-63202474	Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs182514372	chr6:63202479-63202480	Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs538104589	chr6:63202482-63202483	Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs187735384	chr6:63202495-63202496	Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs377215637	chr6:63202516-63202517	Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs111740668	chr6:63202527-63202528	Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs538446191	chr6:63202543-63202544	Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs114584512	chr6:63210646-63210647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs191653583	chr6:63210668-63210669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs76762029	chr6:63210701-63210702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs574692058	chr6:63210704-63210705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs183498011	chr6:63210741-63210742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs60826902	chr6:63210745-63210746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs139984398	chr6:63210811-63210812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs371774849	chr6:63210950-63210951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs187993912	chr6:63210973-63210974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs75105206	chr6:63211041-63211042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs377255455	chr6:63211043-63211044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs532539695	chr6:63211055-63211056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs547856360	chr6:63211066-63211067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs566340605	chr6:63211069-63211070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs536576564	chr6:63211070-63211071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

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
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
Breast cancer	22522925	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	22037309	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:387 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:63201200-63201400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr6:63202200-63202600	Active TSS	HepG2	liver
3	chr6:63210600-63217400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr6:63217400-63217600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr6:63220200-63220400	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr6:63220600-63225000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
7	chr6:63222800-63223200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr6:63223200-63224400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr6:63224400-63224800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr6:63224600-63224800	Enhancers	Cortex derived primary cultured neurospheres	brain
11	chr6:63224600-63225000	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr6:63224600-63226400	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr6:63224800-63225800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr6:63224800-63225800	Weak transcription	Cortex derived primary cultured neurospheres	brain
15	chr6:63225000-63225400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
16	chr6:63225000-63226000	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr6:63225200-63225800	Enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr6:63225400-63226200	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr6:63225400-63226800	Enhancers	iPS-15b Cell Line	embryonic stem cell
20	chr6:63225600-63226200	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr6:63225600-63226200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
22	chr6:63225600-63226200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr6:63225600-63226400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr6:63225600-63226800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr6:63225600-63227400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr6:63225800-63226000	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr6:63225800-63226000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
28	chr6:63225800-63226200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr6:63225800-63226400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr6:63225800-63226400	Enhancers	Primary hematopoietic stem cells short term culture	blood
31	chr6:63225800-63227000	Enhancers	H1 Cell Line	embryonic stem cell
32	chr6:63225800-63227200	Enhancers	Cortex derived primary cultured neurospheres	brain
33	chr6:63226000-63226200	Enhancers	Primary B cells from cord blood	blood
34	chr6:63226000-63226400	Enhancers	iPS-20b Cell Line	embryonic stem cell
35	chr6:63226000-63226800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr6:63226000-63226800	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
37	chr6:63226000-63227000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
38	chr6:63226000-63227000	Enhancers	Primary B cells from peripheral blood	blood
39	chr6:63226000-63227000	Enhancers	Primary hematopoietic stem cells	blood
40	chr6:63226200-63226400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
41	chr6:63226200-63226600	Active TSS	ES-I3 Cell Line	embryonic stem cell
42	chr6:63226200-63226600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr6:63226200-63226600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr6:63226200-63226800	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
45	chr6:63226200-63226800	Flanking Active TSS	Primary B cells from cord blood	blood
46	chr6:63226400-63226600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
47	chr6:63226400-63226800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
48	chr6:63226400-63226800	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr6:63226400-63226800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
50	chr6:63226400-63226800	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood

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