Variant report

Variant	nsv1063895
Chromosome Location	chr20:23715058-23791659
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	ATF1	chr20:23781355-23781508	K562	blood:	n/a	n/a
2	CEBPB	chr20:23715136-23715338	IMR90	lung:	n/a	chr20:23715271-23715282
3	CEBPB	chr20:23779809-23779920	HepG2	liver:	n/a	chr20:23779841-23779854
4	CEBPB	chr20:23786510-23786667	HepG2	liver:	n/a	chr20:23786550-23786561
5	CEBPB	chr20:23747045-23747345	HepG2	liver:	n/a	chr20:23747171-23747182 chr20:23747169-23747180 chr20:23747171-23747180 chr20:23747171-23747180 chr20:23747169-23747182 chr20:23747171-23747180 chr20:23747171-23747180 chr20:23747169-23747182
6	CEBPB	chr20:23747026-23747352	A549	lung:	n/a	chr20:23747171-23747182 chr20:23747169-23747180 chr20:23747171-23747180 chr20:23747029-23747041 chr20:23747171-23747180 chr20:23747169-23747182 chr20:23747171-23747180 chr20:23747171-23747180 chr20:23747169-23747182
7	CEBPB	chr20:23715126-23715326	A549	lung:	n/a	chr20:23715271-23715282
8	CEBPB	chr20:23715133-23715386	HepG2	liver:	n/a	chr20:23715271-23715282
9	CEBPB	chr20:23747142-23747274	K562	blood:	n/a	chr20:23747171-23747182 chr20:23747169-23747180 chr20:23747171-23747180 chr20:23747171-23747180 chr20:23747169-23747182 chr20:23747171-23747180 chr20:23747171-23747180 chr20:23747169-23747182
10	CTCF	chr20:23779884-23780108	SK-N-SH_RA	brain:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
11	CTCF	chr20:23779931-23780147	Spleen_OC	spleen:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
12	CTCF	chr20:23763120-23763270	SAEC	small airway:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
13	CTCF	chr20:23763100-23763250	HVMF	connective:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
14	CTCF	chr20:23763120-23763270	HPF	lung:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
15	CTCF	chr20:23763220-23763370	WI-38	lung:	n/a	n/a
16	CTCF	chr20:23763072-23763323	HepG2	liver:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
17	CTCF	chr20:23763062-23763550	MCF-7	breast:	n/a	chr20:23763450-23763471 chr20:23763448-23763466 chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210 chr20:23763449-23763465
18	CTCF	chr20:23762860-23763010	HFF	foreskin:	n/a	n/a
19	CTCF	chr20:23763140-23763290	K562	blood:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
20	CTCF	chr20:23763120-23763270	HUVEC	blood vessel:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
21	CTCF	chr20:23763080-23763230	BE2_C	brain:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
22	CTCF	chr20:23779920-23780070	GM12869	blood:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
23	CTCF	chr20:23779880-23780030	HVMF	connective:	n/a	n/a
24	CTCF	chr20:23763120-23763270	GM12866	blood:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
25	CTCF	chr20:23763120-23763270	GM12869	blood:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
26	CTCF	chr20:23779820-23779970	WI-38	lung:	n/a	n/a
27	CTCF	chr20:23779900-23780050	NHDF-neo	bronchial:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
28	CTCF	chr20:23763140-23763290	GM12864	blood:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
29	CTCF	chr20:23763240-23763390	HCM	heart:	n/a	n/a
30	CTCF	chr20:23779880-23780030	HEEpiC	esophagus:	n/a	n/a
31	CTCF	chr20:23779899-23780423	H1-hESC	embryonic stem cell:	n/a	chr20:23780275-23780296 chr20:23780274-23780290 chr20:23780320-23780329 chr20:23780273-23780291 chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
32	CTCF	chr20:23763140-23763290	HBMEC	blood vessel:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
33	CTCF	chr20:23779879-23780336	GM19240	blood:	n/a	chr20:23780275-23780296 chr20:23780274-23780290 chr20:23780320-23780329 chr20:23780273-23780291 chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
34	CTCF	chr20:23763090-23763322	Pancreas_OC	pancreas:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
35	CTCF	chr20:23729713-23729903	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr20:23779900-23780050	HA-sp	spinal cord:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
37	CTCF	chr20:23763084-23763290	Spleen_OC	spleen:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
38	CTCF	chr20:23779880-23780030	HPAF	blood vessel:	n/a	n/a
39	CTCF	chr20:23780249-23780347	GM12878	blood:	n/a	chr20:23780275-23780296 chr20:23780274-23780290 chr20:23780320-23780329 chr20:23780273-23780291
40	CTCF	chr20:23763100-23763250	GM06990	blood:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
41	CTCF	chr20:23779880-23780030	HRE	kidney:	n/a	n/a
42	CTCF	chr20:23729601-23729678	GM20000	blood:	n/a	n/a
43	CTCF	chr20:23779960-23780110	HEEpiC	esophagus:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
44	CTCF	chr20:23729517-23729596	H1-hESC	embryonic stem cell:	n/a	n/a
45	CTCF	chr20:23780240-23780390	GM12874	blood:	n/a	chr20:23780275-23780296 chr20:23780274-23780290 chr20:23780320-23780329 chr20:23780273-23780291
46	CTCF	chr20:23729720-23729870	GM12875	blood:	n/a	n/a
47	CTCF	chr20:23780280-23780430	RPTEC	kidney:	n/a	chr20:23780320-23780329
48	CTCF	chr20:23779700-23779850	GM12869	blood:	n/a	n/a
49	CTCF	chr20:23779888-23780427	MCF-7	breast:	n/a	chr20:23780275-23780296 chr20:23780274-23780290 chr20:23780320-23780329 chr20:23780273-23780291 chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
50	CTCF	chr20:23779900-23780050	HFF-Myc	foreskin:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:23732595-23732645	HCPEpiC	choroid plexus:	n/a
2	chr20:23732595-23732645	HCPEpiC	choroid plexus:	n/a
3	chr20:23728432-23728482	K562	blood:	n/a
4	chr20:23728814-23728864	SK-N-SH_RA	brain:	n/a
5	chr20:23728432-23728482	ECC-1	luminal epithelium:	n/a
6	chr20:23731367-23731417	CMK	blood:	n/a
7	chr20:23732595-23732645	HPAEpiC	pulmonary alveolar:	n/a
8	chr20:23732595-23732645	HRPEpiC	eye:	n/a
9	chr20:23732595-23732645	IMR90	lung:	fetal
10	chr20:23728814-23728864	HCT-116	colon:	n/a
11	chr20:23728814-23728864	CMK	blood:	n/a
12	chr20:23728432-23728482	HCF	heart:	n/a
13	chr20:23732595-23732645	SK-N-MC	brain:	n/a
14	chr20:23731367-23731417	PrEC	prostate:	n/a
15	chr20:23732873-23732923	AG09319	gingival:	n/a
16	chr20:23732873-23732923	Caco-2	colon:	n/a
17	chr20:23732595-23732645	AG04450	lung:	fetal
18	chr20:23732595-23732645	GM19239	blood:	n/a
19	chr20:23728432-23728482	AG04449	skin:	fetal
20	chr20:23732873-23732923	LNCaP	prostate:	n/a
21	chr20:23732873-23732923	HCT-116	colon:	n/a
22	chr20:23731367-23731417	SAEC	small airway:	n/a
23	chr20:23732595-23732645	HRE	kidney:	n/a
24	chr20:23731367-23731417	HIPEpiC	eye:	n/a
25	chr20:23728814-23728864	MCF10A-Er-Src	breast:	n/a
26	chr20:23732595-23732645	BE2_C	brain:	n/a
27	chr20:23728432-23728482	NH-A	brain:	n/a
28	chr20:23728432-23728482	Hela-S3	cervix:	n/a
29	chr20:23731367-23731417	Caco-2	colon:	n/a
30	chr20:23732595-23732645	NT2-D1	testis:	n/a
31	chr20:23731367-23731417	ECC-1	luminal epithelium:	n/a
32	chr20:23732595-23732645	HL-60	blood:	n/a
33	chr20:23728432-23728482	U87	brain:	n/a
34	chr20:23732873-23732923	HRE	kidney:	n/a
35	chr20:23731367-23731417	AG09319	gingival:	n/a
36	chr20:23728432-23728482	HL-60	blood:	n/a
37	chr20:23728814-23728864	AG04450	lung:	fetal
38	chr20:23728432-23728482	H1-hESC	embryonic stem cell:	embryo
39	chr20:23731367-23731417	PANC-1	pancreas:	n/a
40	chr20:23732873-23732923	AG04449	skin:	fetal
41	chr20:23728432-23728482	MCF10A-Er-Src	breast:	n/a
42	chr20:23728814-23728864	AG04449	skin:	fetal
43	chr20:23728432-23728482	HMEC	breast:	n/a
44	chr20:23732873-23732923	IMR90	lung:	fetal
45	chr20:23732873-23732923	NT2-D1	testis:	n/a
46	chr20:23728814-23728864	HCM	heart:	n/a
47	chr20:23732873-23732923	K562	blood:	n/a
48	chr20:23732873-23732923	ECC-1	luminal epithelium:	n/a
49	chr20:23732595-23732645	MCF-7	breast:	n/a
50	chr20:23732595-23732645	HepG2	liver:	n/a

No.	Distal block	Cell Line	Cell type
1	chr20:23704352..23705295-chr20:23754423..23755304,4	MCF-7	breast:
2	chr20:23704491..23705478-chr20:23779622..23780975,4	MCF-7	breast:
3	chr20:23704490..23705249-chr20:23762654..23763235,2	MCF-7	breast:
4	chr20:23779275..23780409-chr20:23837370..23837992,3	MCF-7	breast:
5	chr20:23649188..23649689-chr20:23762769..23763504,2	MCF-7	breast:
6	chr20:23645187..23645712-chr20:23775888..23776677,2	MCF-7	breast:
7	chr20:23779854..23780390-chr20:23870001..23870554,2	MCF-7	breast:
8	chr20:23648767..23649721-chr20:23779902..23780425,2	MCF-7	breast:
9	chr20:23702805..23703439-chr20:23754485..23755364,2	MCF-7	breast:
10	chr20:23763057..23763763-chr20:23870036..23871243,3	MCF-7	breast:
11	chr20:23754506..23755505-chr20:23837367..23838288,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CST8-5	chr20:23733160-23733281	NONHSAT079083
2	lnc-CST8-3	chr20:23785871-23786300	XLOC_013494
3	lnc-CST8-5	chr20:23726778-23726924	NONHSAT079083
4	lnc-CST8-5	chr20:23732376-23732473	NONHSAT079083
5	lnc-CST8-5	chr20:23733871-23734300	NONHSAT079083
6	lnc-CST8-3	chr20:23785160-23785281	XLOC_013494
7	lnc-CST8-3	chr20:23778778-23778924	XLOC_013494
8	lnc-CST8-3	chr20:23784376-23784473	XLOC_013494

Variant related genes	Relation type
ENSG00000230908	TF binding region
CST1	TF binding region
ENSG00000230908	CpG island
CST1	CpG island
XIAP	miRNA target sites
WWC2	miRNA target sites
WWP2	miRNA target sites

Extended variants
information (count: 2693 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:2693 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs186642583	chr20:23715080-23715081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs59412818	chr20:23715164-23715165	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs536628367	chr20:23715168-23715169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs557266996	chr20:23715173-23715174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs567985277	chr20:23715204-23715205	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs116968187	chr20:23715206-23715207	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs536872956	chr20:23715213-23715214	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs150999319	chr20:23715217-23715218	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs142343447	chr20:23715237-23715238	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs539180715	chr20:23715250-23715251	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs144664819	chr20:23715251-23715252	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs75841856	chr20:23715272-23715273	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs539007256	chr20:23715278-23715279	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs544581385	chr20:23715315-23715316	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs61300577	chr20:23715320-23715321	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs6106700	chr20:23715329-23715330	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs542819813	chr20:23715341-23715342	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs147873839	chr20:23715372-23715373	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs141680072	chr20:23715382-23715383	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs528288062	chr20:23715391-23715392	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs551092305	chr20:23715405-23715406	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs191050047	chr20:23715420-23715421	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs183191764	chr20:23715422-23715423	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs550133578	chr20:23715426-23715427	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs567952576	chr20:23715434-23715435	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs188499897	chr20:23715437-23715438	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs547267569	chr20:23715438-23715439	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs114386504	chr20:23715454-23715455	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs193058135	chr20:23715459-23715460	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs150422743	chr20:23715471-23715472	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs4600728	chr20:23715485-23715486	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs538244396	chr20:23715489-23715490	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs55931913	chr20:23715490-23715491	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs4629231	chr20:23715496-23715497	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
35	rs544514127	chr20:23715497-23715498	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs374443147	chr20:23715517-23715518	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs559578838	chr20:23715530-23715531	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs562724501	chr20:23715534-23715535	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs544770908	chr20:23715535-23715536	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs114577793	chr20:23715539-23715540	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs61065813	chr20:23715557-23715558	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs532065866	chr20:23715567-23715568	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs550251770	chr20:23715568-23715569	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs560767733	chr20:23715569-23715570	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs550222983	chr20:23715570-23715571	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs143396848	chr20:23715571-23715572	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs139042367	chr20:23715593-23715594	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs567117001	chr20:23715594-23715595	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs184843710	chr20:23715609-23715610	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs552756237	chr20:23715640-23715641	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
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
Renal cell carcinoma	18765545	CNVD
Alagille syndrome	17576883	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Breast cancer	16608533	CNVD
Bladder cancer	21909424	CNVD
Esophageal cancer	21851588	CNVD
Breast cancer	17133270	CNVD
Thrombophilia	17576883	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	21062444	CNVD
Hepatocellular carcinoma	22174799	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Chordoma	18071362	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
small cell lung cancer	17426248	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:205 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:23714200-23719000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr20:23715200-23716000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr20:23715400-23716400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr20:23719000-23719400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr20:23724800-23726600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr20:23725200-23726800	Enhancers	HUVEC	blood vessel
7	chr20:23725400-23725800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr20:23725400-23725800	Enhancers	Osteobl	bone
9	chr20:23725400-23726000	Enhancers	NHLF	lung
10	chr20:23725400-23726600	Enhancers	NHDF-Ad	bronchial
11	chr20:23725400-23727000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr20:23725600-23725800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr20:23725800-23726200	Enhancers	Muscle Satellite Cultured Cells	--
14	chr20:23725800-23727000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr20:23726800-23727000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr20:23726800-23731800	Weak transcription	HUVEC	blood vessel
17	chr20:23727000-23727200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr20:23727000-23729600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr20:23727200-23727800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr20:23727800-23728000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr20:23727800-23728400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr20:23727800-23728600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr20:23727800-23728800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
24	chr20:23728000-23728600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr20:23728600-23728800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr20:23728600-23729200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr20:23728800-23731400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr20:23728800-23735000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr20:23729200-23730600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr20:23729600-23734400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr20:23730600-23730800	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr20:23730600-23731000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
33	chr20:23730800-23731000	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr20:23730800-23731600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr20:23731000-23731200	Enhancers	H9 Cell Line	embryonic stem cell
36	chr20:23731000-23732000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr20:23731200-23731400	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
38	chr20:23731400-23731600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
39	chr20:23731600-23733600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr20:23731800-23732000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr20:23731800-23732200	Enhancers	HUVEC	blood vessel
42	chr20:23732000-23732800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr20:23732200-23734200	Weak transcription	HUVEC	blood vessel
44	chr20:23732600-23734000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr20:23732800-23733200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr20:23733200-23733600	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr20:23733600-23737000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
48	chr20:23733800-23736600	Enhancers	NHDF-Ad	bronchial
49	chr20:23733800-23736800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr20:23734000-23736400	Enhancers	Muscle Satellite Cultured Cells	--

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