Variant report

Variant	nsv529577
Chromosome Location	chr20:14434373-14799157
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1696)
CpG islands
(count:0)
Chromatin interactive
region (count:36)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1696 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr20:14590214-14590575	HepG2	liver:	n/a	n/a
2	ATF1	chr20:14706954-14707154	K562	blood:	n/a	n/a
3	ATF2	chr20:14519085-14519448	GM12878	blood:	n/a	n/a
4	ATF2	chr20:14725297-14725726	GM12878	blood:	n/a	n/a
5	ATF3	chr20:14613673-14613899	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF3	chr20:14613539-14613866	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF3	chr20:14603385-14603865	A549	lung:	n/a	n/a
8	ATF3	chr20:14692815-14693406	A549	lung:	n/a	n/a
9	BACH1	chr20:14702858-14702913	K562	blood:	n/a	n/a
10	BACH1	chr20:14548845-14549180	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr20:14549483-14549672	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr20:14470918-14471200	GM12878	blood:	n/a	chr20:14471085-14471095 chr20:14471084-14471095
13	BATF	chr20:14725428-14725715	GM12878	blood:	n/a	n/a
14	BATF	chr20:14519115-14519423	GM12878	blood:	n/a	n/a
15	BATF	chr20:14782350-14782619	GM12878	blood:	n/a	chr20:14782584-14782592
16	BATF	chr20:14704304-14704567	GM12878	blood:	n/a	n/a
17	BATF	chr20:14704765-14705024	GM12878	blood:	n/a	n/a
18	BATF	chr20:14725407-14725742	GM12878	blood:	n/a	n/a
19	BCL11A	chr20:14519112-14519442	GM12878	blood:	n/a	n/a
20	BCL11A	chr20:14519106-14519411	GM12878	blood:	n/a	n/a
21	BCL3	chr20:14692841-14693476	A549	lung:	n/a	chr20:14693105-14693113
22	BCL3	chr20:14681041-14681305	GM12878	blood:	n/a	n/a
23	BCL3	chr20:14681045-14681280	GM12878	blood:	n/a	n/a
24	BHLHE40	chr20:14560713-14560743	A549	lung:	n/a	n/a
25	BHLHE40	chr20:14519061-14519462	GM12878	blood:	n/a	n/a
26	BHLHE40	chr20:14704309-14704573	GM12878	blood:	n/a	n/a
27	BHLHE40	chr20:14680806-14681273	GM12878	blood:	n/a	n/a
28	BHLHE40	chr20:14516100-14516128	GM12878	blood:	n/a	n/a
29	BHLHE40	chr20:14672674-14672924	GM12878	blood:	n/a	n/a
30	BRCA1	chr20:14605458-14605460	H1-hESC	embryonic stem cell:	n/a	n/a
31	BRCA1	chr20:14477554-14478434	Hela-S3	cervix:	n/a	n/a
32	BRCA1	chr20:14564058-14564490	Hela-S3	cervix:	n/a	n/a
33	BRCA1	chr20:14462597-14462814	Hela-S3	cervix:	n/a	n/a
34	BRCA1	chr20:14534754-14535183	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr20:14471046-14471218	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr20:14779516-14779580	H1-hESC	embryonic stem cell:	n/a	chr20:14779546-14779557
37	CEBPB	chr20:14603468-14603827	A549	lung:	n/a	n/a
38	CEBPB	chr20:14653868-14654331	A549	lung:	n/a	n/a
39	CEBPB	chr20:14590238-14590540	HepG2	liver:	n/a	n/a
40	CEBPB	chr20:14456905-14457062	HepG2	liver:	n/a	chr20:14456912-14456923
41	CEBPB	chr20:14756937-14757139	A549	lung:	n/a	n/a
42	CEBPB	chr20:14667957-14668265	Hela-S3	cervix:	n/a	chr20:14668099-14668110 chr20:14668097-14668108
43	CEBPB	chr20:14708440-14708728	IMR90	lung:	n/a	chr20:14708579-14708590
44	CEBPB	chr20:14468942-14469246	HepG2	liver:	n/a	chr20:14469139-14469152 chr20:14469139-14469150 chr20:14469078-14469089 chr20:14469139-14469150 chr20:14469075-14469092 chr20:14469078-14469091
45	CEBPB	chr20:14692969-14693530	MCF-7	breast:	n/a	n/a
46	CEBPB	chr20:14593036-14593433	A549	lung:	n/a	chr20:14593419-14593430 chr20:14593214-14593225 chr20:14593417-14593430 chr20:14593419-14593430
47	CEBPB	chr20:14462739-14462794	A549	lung:	n/a	n/a
48	CEBPB	chr20:14563488-14563850	HepG2	liver:	n/a	chr20:14563664-14563675
49	CEBPB	chr20:14677983-14678307	HepG2	liver:	n/a	chr20:14678123-14678134 chr20:14678124-14678133 chr20:14678122-14678135 chr20:14678122-14678133
50	CEBPB	chr20:14590237-14590495	HepG2	liver:	n/a	n/a

No data

(count:36 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr20:14741627..14743404-chr20:14744142..14746208,2	MCF-7	breast:
2	chr20:14741627..14743404-chr20:14744142..14746208,2	MCF-7	breast:
3	chr20:14593902..14596386-chr20:15052997..15054796,2	K562	blood:
4	chr20:14688944..14691499-chr20:14692203..14695103,3	MCF-7	breast:
5	chr20:14487196..14489290-chr20:14493950..14495618,2	MCF-7	breast:
6	chr20:14755716..14758614-chr20:14760211..14762111,2	MCF-7	breast:
7	chr20:14767717..14771762-chr20:14774616..14777473,4	MCF-7	breast:
8	chr20:14733858..14735719-chr20:14744279..14746694,2	MCF-7	breast:
9	chr20:14743071..14745118-chr20:14745452..14747052,2	K562	blood:
10	chr20:14725880..14727683-chr20:14729457..14731582,2	MCF-7	breast:
11	chr20:14743071..14745118-chr20:14745452..14747052,2	K562	blood:
12	chr20:14601339..14605162-chr20:14611440..14614800,3	MCF-7	breast:
13	chr20:14512165..14513979-chr20:14521499..14523425,2	MCF-7	breast:
14	chr20:14744879..14746579-chr20:14747938..14749575,2	MCF-7	breast:
15	chr20:14767717..14771762-chr20:14774616..14777473,4	MCF-7	breast:
16	chr20:14733858..14735719-chr20:14744279..14746694,2	MCF-7	breast:
17	chr20:14757945..14761170-chr20:14762279..14765371,3	MCF-7	breast:
18	chr20:14469605..14471318-chr20:14479870..14481906,2	MCF-7	breast:
19	chr20:14657146..14658733-chr20:17661268..17663723,2	MCF-7	breast:
20	chr20:14705956..14708856-chr20:14709274..14711884,2	K562	blood:
21	chr20:14725880..14727683-chr20:14729457..14731582,2	MCF-7	breast:
22	chr20:14705956..14708856-chr20:14709274..14711884,2	K562	blood:
23	chr20:14769951..14772584-chr20:14781634..14783463,2	MCF-7	breast:
24	chr20:14487196..14489290-chr20:14493950..14495618,2	MCF-7	breast:
25	chr20:14744879..14746579-chr20:14747938..14749575,2	MCF-7	breast:
26	chr20:14512165..14513979-chr20:14521499..14523425,2	MCF-7	breast:
27	chr20:14769951..14772584-chr20:14781634..14783463,2	MCF-7	breast:
28	chr20:14606804..14608358-chr20:14690132..14692728,2	MCF-7	breast:
29	chr20:12959607..12961682-chr20:14555879..14557670,2	K562	blood:
30	chr20:14755716..14758614-chr20:14760211..14762111,2	MCF-7	breast:
31	chr20:14688944..14691499-chr20:14692203..14695103,3	MCF-7	breast:
32	chr19:30441690..30442493-chr20:14547650..14548282,2	MCF-7	breast:
33	chr20:14469605..14471318-chr20:14479870..14481906,2	MCF-7	breast:
34	chr20:14601339..14605162-chr20:14611440..14614800,3	MCF-7	breast:
35	chr20:14757945..14761170-chr20:14762279..14765371,3	MCF-7	breast:
36	chr20:14527106..14529484-chr20:14530662..14532376,3	MCF-7	breast:

(count:15 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C20orf7-1	chr20:14603520-14603660	ENSG00000227927.1
2	lnc-C20orf7-1	chr20:14617092-14617170	ENSG00000227927.2
3	lnc-C20orf7-1	chr20:14535030-14535074	ENSG00000227927.1
4	lnc-FLRT3-3	chr20:14527830-14528269	NONHSAT078717
5	lnc-C20orf7-3	chr20:14504044-14504100	NONHSAT078716
6	lnc-C20orf7-1	chr20:14609283-14609475	ENSG00000227927.2
7	lnc-C20orf7-3	chr20:14665489-14665605	NONHSAT078716
8	lnc-C20orf7-1	chr20:14607559-14607752	ENSG00000227927.2
9	lnc-C20orf7-3	chr20:14474125-14474154	NONHSAT078714
10	lnc-C20orf7-4	chr20:14591719-14595690	NONHSAT078719
11	lnc-C20orf7-1	chr20:14609283-14609554	ENSG00000227927.1
12	lnc-C20orf7-1	chr20:14612487-14612595	ENSG00000227927.2
13	lnc-C20orf7-1	chr20:14607710-14607752	ENSG00000227927.1
14	lnc-C20orf7-1	chr20:14602412-14602575	ENSG00000227927.1
15	lnc-C20orf7-3	chr20:14665489-14665605	NONHSAT078714

No data

Variant related genes	Relation type
MACROD2	TF binding region
RPS10P2	TF binding region
ENSG00000227563	TF binding region
MACROD2-IT1	TF binding region
ENSG00000227927	chromatin interactions
ENSG00000125844	chromatin interactions
ENSG00000227563	chromatin interactions

Extended variants
information (count: 10853 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:10853 , 50 per page) page: 1 2 3 4 5 6 7 ... 218

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6079449	chr20:14434383-14434384	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs143365562	chr20:14434546-14434547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs6135150	chr20:14434555-14434556	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs566754875	chr20:14434578-14434579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs62204403	chr20:14434607-14434608	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs187963135	chr20:14434687-14434688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs532727869	chr20:14434799-14434800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs552434856	chr20:14434872-14434873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs566164700	chr20:14434876-14434877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs534768409	chr20:14434908-14434909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs138943416	chr20:14434971-14434972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs568083921	chr20:14435016-14435017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs56799693	chr20:14435064-14435065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs575465815	chr20:14435072-14435073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs397799304	chr20:14435075-14435076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs192438973	chr20:14435126-14435127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs117743890	chr20:14435201-14435202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs372024618	chr20:14435257-14435258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs184414159	chr20:14435328-14435329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs111833167	chr20:14435352-14435353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs112821013	chr20:14435376-14435377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs75833837	chr20:14435395-14435396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs11087091	chr20:14435416-14435417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs7264094	chr20:14435419-14435420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs541534479	chr20:14435425-14435426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs192511053	chr20:14435450-14435451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs575295264	chr20:14435487-14435488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs574027903	chr20:14435491-14435492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs184546928	chr20:14435492-14435493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs574849575	chr20:14435495-14435496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs542634578	chr20:14435499-14435500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs532647315	chr20:14435503-14435504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs559654788	chr20:14435525-14435526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs552747097	chr20:14435561-14435562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs7264063	chr20:14435562-14435563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs142279769	chr20:14435584-14435585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs528606145	chr20:14435600-14435601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs188934662	chr20:14435633-14435634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs181475264	chr20:14435634-14435635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs186476393	chr20:14435641-14435642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs550514292	chr20:14435646-14435647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs570734008	chr20:14435659-14435660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs146383209	chr20:14435690-14435691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs573218620	chr20:14435695-14435696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs189777621	chr20:14435730-14435731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs572932219	chr20:14435764-14435765	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs369459079	chr20:14435765-14435766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs13037191	chr20:14435786-14435787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs13037192	chr20:14435788-14435789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs13045714	chr20:14435818-14435819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:73)

Disease	PMID	Source
Breast cancer	16397240	CNVD
abortions and stillbirths	19751515	CNVD
Wilms tumour	21544195	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	16272173	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	19627613	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Colorectal cancer	19359472	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Central neurocytomas	17123091	CNVD
Colorectal cancer	16272173	CNVD
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Colorectal cancer	21645411	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Autism	22495311	CNVD
Glaucoma	21310917	CNVD
Alagille syndrome	22470819	CNVD
Lung cancer	16773561	CNVD
Renal cell carcinoma	18765545	CNVD
Alagille syndrome	17576883	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
Prostate cancer	18632612	CNVD
Ewing''s sarcoma	18628472	CNVD
Glioblastoma multiforme	18628472	CNVD
Leukemia	18628472	CNVD
Myelofibrosis	22110671	CNVD
Kabuki syndrome	21720541	CNVD
Glioblastoma multiforme	22286061	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Neurocytoma	17123091	CNVD
Glioblastoma multiforme	21138945	CNVD
Cancer	20164919	CNVD
Multiple sclerosis	20663923	CNVD
Schizophrenia	20663923	CNVD
brain infarct	20663923	CNVD
Breast cancer	22522925	CNVD
Breast cancer	17142309	CNVD
Cancer	20164920	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Autism	20531469	CNVD
Schizophrenia	20967226	CNVD
Williams Syndrome	20824207	CNVD
Melanoma	17363583	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
early-passage human iPS cells	21368824	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD

Chromatin state (count:1127 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:14434000-14434400	Enhancers	Fetal Kidney	kidney
2	chr20:14434200-14437400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr20:14437400-14437600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr20:14444600-14451200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr20:14447600-14451000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr20:14447800-14448200	Active TSS	Gastric	stomach
7	chr20:14447800-14448200	Active TSS	Pancreas	Pancrea
8	chr20:14447800-14448400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
9	chr20:14447800-14448400	Active TSS	Colonic Mucosa	Colon
10	chr20:14447800-14448400	Active TSS	Rectal Mucosa Donor 29	rectum
11	chr20:14447800-14448400	Active TSS	A549	lung
12	chr20:14448000-14448200	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr20:14448000-14448200	Active TSS	Rectal Mucosa Donor 31	rectum
14	chr20:14448000-14448400	Active TSS	Duodenum Mucosa	Duodenum
15	chr20:14448000-14448400	Active TSS	Stomach Mucosa	stomach
16	chr20:14448000-14448400	Enhancers	HepG2	liver
17	chr20:14448200-14448400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr20:14448200-14448400	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
19	chr20:14448200-14450800	Weak transcription	Gastric	stomach
20	chr20:14448200-14450800	Weak transcription	Pancreas	Pancrea
21	chr20:14448200-14451600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
22	chr20:14448400-14448600	Enhancers	Stomach Mucosa	stomach
23	chr20:14448400-14448600	Flanking Active TSS	A549	lung
24	chr20:14448400-14450800	Weak transcription	Duodenum Mucosa	Duodenum
25	chr20:14448400-14450800	Weak transcription	Rectal Mucosa Donor 31	rectum
26	chr20:14448400-14450800	Weak transcription	HepG2	liver
27	chr20:14448400-14451000	Weak transcription	Colonic Mucosa	Colon
28	chr20:14448400-14451000	Weak transcription	Rectal Mucosa Donor 29	rectum
29	chr20:14448400-14451200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr20:14448600-14450800	Weak transcription	Stomach Mucosa	stomach
31	chr20:14448600-14450800	Weak transcription	A549	lung
32	chr20:14450400-14450800	Enhancers	Liver	Liver
33	chr20:14450800-14451200	Enhancers	Rectal Mucosa Donor 31	rectum
34	chr20:14450800-14451200	Enhancers	Sigmoid Colon	Sigmoid Colon
35	chr20:14450800-14451400	Flanking Active TSS	Liver	Liver
36	chr20:14450800-14451400	Enhancers	Stomach Mucosa	stomach
37	chr20:14450800-14451400	Flanking Active TSS	A549	lung
38	chr20:14450800-14451400	Flanking Active TSS	HepG2	liver
39	chr20:14450800-14451800	Enhancers	Duodenum Mucosa	Duodenum
40	chr20:14450800-14451800	Enhancers	Fetal Intestine Small	intestine
41	chr20:14450800-14451800	Enhancers	Gastric	stomach
42	chr20:14450800-14452000	Enhancers	Fetal Intestine Large	intestine
43	chr20:14450800-14452000	Enhancers	Pancreas	Pancrea
44	chr20:14450800-14452200	Enhancers	H1 Cell Line	embryonic stem cell
45	chr20:14450800-14452800	Enhancers	iPS-15b Cell Line	embryonic stem cell
46	chr20:14450800-14461400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr20:14451000-14451200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
48	chr20:14451000-14451600	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr20:14451000-14451600	Enhancers	Colonic Mucosa	Colon
50	chr20:14451000-14451600	Enhancers	Rectal Mucosa Donor 29	rectum

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links