Variant report

Variant	nsv1065355
Chromosome Location	chr20:23725528-23796651
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	chr20:23747026-23747352	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
3	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
4	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
5	CEBPB	chr20:23779809-23779920	HepG2	liver:	n/a	chr20:23779841-23779854
6	CEBPB	chr20:23786510-23786667	HepG2	liver:	n/a	chr20:23786550-23786561
7	CTCF	chr20:23779831-23780203	IMR90	lung:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
8	CTCF	chr20:23763015-23763537	SK-N-SH	brain:	n/a	chr20:23763450-23763471 chr20:23763448-23763466 chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210 chr20:23763449-23763465
9	CTCF	chr20:23756440-23756590	GM12867	blood:	n/a	n/a
10	CTCF	chr20:23779213-23779220	MCF-7	breast:	n/a	n/a
11	CTCF	chr20:23779845-23780154	T-47D	breast:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
12	CTCF	chr20:23779879-23780428	HepG2	liver:	n/a	chr20:23780275-23780296 chr20:23780274-23780290 chr20:23780320-23780329 chr20:23780273-23780291 chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
13	CTCF	chr20:23729640-23729790	HepG2	liver:	n/a	n/a
14	CTCF	chr20:23779960-23780110	Hela-S3	cervix:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
15	CTCF	chr20:23779912-23780152	Hela-S3	cervix:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
16	CTCF	chr20:23763100-23763250	GM12874	blood:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
17	CTCF	chr20:23779880-23780030	HCFaa	heart:	n/a	n/a
18	CTCF	chr20:23779960-23780110	HepG2	liver:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
19	CTCF	chr20:23742005-23742067	Lung_OC	lung:	n/a	n/a
20	CTCF	chr20:23779960-23780110	WERI-Rb-1	eye:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
21	CTCF	chr20:23779833-23780212	GM12878	blood:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
22	CTCF	chr20:23729713-23729903	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr20:23779960-23780110	HMEC	breast:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
24	CTCF	chr20:23763080-23763230	HRPEpiC	eye:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
25	CTCF	chr20:23780260-23780410	MCF-7	breast:	n/a	chr20:23780275-23780296 chr20:23780274-23780290 chr20:23780320-23780329 chr20:23780273-23780291
26	CTCF	chr20:23763120-23763270	GM12875	blood:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
27	CTCF	chr20:23780240-23780390	GM12872	blood:	n/a	chr20:23780275-23780296 chr20:23780274-23780290 chr20:23780320-23780329 chr20:23780273-23780291
28	CTCF	chr20:23763069-23763071	HepG2	liver:	n/a	n/a
29	CTCF	chr20:23763023-23763369	A549	lung:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
30	CTCF	chr20:23779886-23780187	GM12878	blood:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
31	CTCF	chr20:23779960-23780110	AG09309	skin:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
32	CTCF	chr20:23729760-23729910	K562	blood:	n/a	n/a
33	CTCF	chr20:23729640-23729790	HBMEC	blood vessel:	n/a	n/a
34	CTCF	chr20:23763120-23763270	HUVEC	blood vessel:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
35	CTCF	chr20:23754975-23755015	LNCaP	prostate:	n/a	chr20:23754976-23754989
36	CTCF	chr20:23763324-23763334	HepG2	liver:	n/a	n/a
37	CTCF	chr20:23779980-23780130	MCF-7	breast:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
38	CTCF	chr20:23763116-23763277	SK-N-SH_RA	brain:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
39	CTCF	chr20:23779880-23780030	GM12875	blood:	n/a	n/a
40	CTCF	chr20:23763100-23763250	GM12868	blood:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
41	CTCF	chr20:23763120-23763270	AG04450	lung:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
42	CTCF	chr20:23763160-23763310	HRE	kidney:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
43	CTCF	chr20:23779847-23780154	HepG2	liver:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
44	CTCF	chr20:23779900-23780050	HFF-Myc	foreskin:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
45	CTCF	chr20:23779896-23780383	ProgFib	skin:	n/a	chr20:23780275-23780296 chr20:23780274-23780290 chr20:23780320-23780329 chr20:23780273-23780291 chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
46	CTCF	chr20:23780280-23780430	HUVEC	blood vessel:	n/a	chr20:23780320-23780329
47	CTCF	chr20:23779960-23780110	SK-N-SH_RA	brain:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
48	CTCF	chr20:23763083-23763318	GM19239	blood:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
49	CTCF	chr20:23756679-23756838	K562	blood:	n/a	chr20:23756767-23756780
50	CTCF	chr20:23756600-23756750	HRE	kidney:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:23732873-23732923	NB4	blood:	n/a
2	chr20:23732873-23732923	HAEpiC	amniotic membrane:	n/a
3	chr20:23731367-23731417	A549	lung:	n/a
4	chr20:23732873-23732923	HEEpiC	esophagus:	n/a
5	chr20:23728432-23728482	U87	brain:	n/a
6	chr20:23731367-23731417	SKMC	muscle:	n/a
7	chr20:23731367-23731417	GM12892	blood:	n/a
8	chr20:23731367-23731417	HEEpiC	esophagus:	n/a
9	chr20:23731367-23731417	HPAEpiC	pulmonary alveolar:	n/a
10	chr20:23731367-23731417	PFSK-1	brain:	n/a
11	chr20:23731367-23731417	K562	blood:	n/a
12	chr20:23728814-23728864	LNCaP	prostate:	n/a
13	chr20:23728432-23728482	SKMC	muscle:	n/a
14	chr20:23732873-23732923	U87	brain:	n/a
15	chr20:23728814-23728864	BE2_C	brain:	n/a
16	chr20:23732873-23732923	RPTEC	kidney:	n/a
17	chr20:23728814-23728864	HEEpiC	esophagus:	n/a
18	chr20:23728814-23728864	NT2-D1	testis:	n/a
19	chr20:23732595-23732645	H1-hESC	embryonic stem cell:	embryo
20	chr20:23732595-23732645	ProgFib	skin:	n/a
21	chr20:23731367-23731417	HIPEpiC	eye:	n/a
22	chr20:23732595-23732645	MCF10A-Er-Src	breast:	n/a
23	chr20:23728814-23728864	AoSMC	blood vessel:	n/a
24	chr20:23731367-23731417	HUVEC	blood vessel:	n/a
25	chr20:23728814-23728864	A549	lung:	n/a
26	chr20:23728814-23728864	RPTEC	kidney:	n/a
27	chr20:23728432-23728482	ECC-1	luminal epithelium:	n/a
28	chr20:23728814-23728864	NH-A	brain:	n/a
29	chr20:23728432-23728482	SK-N-SH_RA	brain:	n/a
30	chr20:23731367-23731417	AG09319	gingival:	n/a
31	chr20:23732873-23732923	HepG2	liver:	n/a
32	chr20:23728432-23728482	HMEC	breast:	n/a
33	chr20:23728814-23728864	HepG2	liver:	n/a
34	chr20:23732595-23732645	HepG2	liver:	n/a
35	chr20:23732595-23732645	HIPEpiC	eye:	n/a
36	chr20:23732873-23732923	A549	lung:	n/a
37	chr20:23732595-23732645	HMEC	breast:	n/a
38	chr20:23732595-23732645	HUVEC	blood vessel:	n/a
39	chr20:23728432-23728482	HAEpiC	amniotic membrane:	n/a
40	chr20:23728814-23728864	HNPCEpiC	eye:	n/a
41	chr20:23728814-23728864	H1-hESC	embryonic stem cell:	embryo
42	chr20:23728432-23728482	HIPEpiC	eye:	n/a
43	chr20:23731367-23731417	ovcar-3	ovarian:	n/a
44	chr20:23731367-23731417	MCF10A-Er-Src	breast:	n/a
45	chr20:23728814-23728864	HUVEC	blood vessel:	n/a
46	chr20:23731367-23731417	MCF-7	breast:	n/a
47	chr20:23732595-23732645	AG09319	gingival:	n/a
48	chr20:23728432-23728482	CMK	blood:	n/a
49	chr20:23728814-23728864	Jurkat	blood:	n/a
50	chr20:23728814-23728864	ProgFib	skin:	n/a

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

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

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

Extended variants
information (count: 2553 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:2553 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6049057	chr20:23725528-23725529	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs193252347	chr20:23725572-23725573	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs545691879	chr20:23725600-23725601	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs116299389	chr20:23725695-23725696	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs370020309	chr20:23725702-23725703	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs562063139	chr20:23725704-23725705	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs6049058	chr20:23725705-23725706	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs531148682	chr20:23725727-23725728	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs375846574	chr20:23725760-23725761	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs529260447	chr20:23725777-23725778	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs71333776	chr20:23725804-23725805	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs143257787	chr20:23725805-23725806	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs35732685	chr20:23725806-23725807	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs532358214	chr20:23725816-23725817	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs533593347	chr20:23725838-23725839	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs114443772	chr20:23725852-23725853	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs6036513	chr20:23725888-23725889	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs200474075	chr20:23725924-23725925	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs536932722	chr20:23725934-23725935	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs567184610	chr20:23725952-23725953	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs571565035	chr20:23725955-23725956	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs118084386	chr20:23725968-23725969	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs148294002	chr20:23725982-23725983	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs140511309	chr20:23726048-23726049	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs552751793	chr20:23726164-23726165	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs572798310	chr20:23726184-23726185	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs185321829	chr20:23726225-23726226	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs369493541	chr20:23726226-23726227	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs559306399	chr20:23726237-23726238	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs576039839	chr20:23726238-23726239	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs6049060	chr20:23726242-23726243	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs190172346	chr20:23726295-23726296	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs535042569	chr20:23726308-23726309	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs114207825	chr20:23726316-23726317	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs117301435	chr20:23726318-23726319	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs114877843	chr20:23726322-23726323	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs375614114	chr20:23726326-23726327	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs117730889	chr20:23726329-23726330	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs568890500	chr20:23726330-23726331	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs530760551	chr20:23726370-23726371	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs550450399	chr20:23726383-23726384	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs376169196	chr20:23726397-23726398	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs147053817	chr20:23726435-23726436	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs536011573	chr20:23726466-23726467	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs553053174	chr20:23726485-23726486	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs573142030	chr20:23726490-23726491	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs566409181	chr20:23726498-23726499	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs138485177	chr20:23726499-23726500	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs72490823	chr20:23726523-23726524	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs143944683	chr20:23726542-23726543	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:204 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:23724800-23726600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr20:23725200-23726800	Enhancers	HUVEC	blood vessel
3	chr20:23725400-23725800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr20:23725400-23725800	Enhancers	Osteobl	bone
5	chr20:23725400-23726000	Enhancers	NHLF	lung
6	chr20:23725400-23726600	Enhancers	NHDF-Ad	bronchial
7	chr20:23725400-23727000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr20:23725600-23725800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr20:23725800-23726200	Enhancers	Muscle Satellite Cultured Cells	--
10	chr20:23725800-23727000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr20:23726800-23727000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr20:23726800-23731800	Weak transcription	HUVEC	blood vessel
13	chr20:23727000-23727200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr20:23727000-23729600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr20:23727200-23727800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr20:23727800-23728000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr20:23727800-23728400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr20:23727800-23728600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr20:23727800-23728800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr20:23728000-23728600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr20:23728600-23728800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr20:23728600-23729200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr20:23728800-23731400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr20:23728800-23735000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr20:23729200-23730600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr20:23729600-23734400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr20:23730600-23730800	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr20:23730600-23731000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
29	chr20:23730800-23731000	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr20:23730800-23731600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr20:23731000-23731200	Enhancers	H9 Cell Line	embryonic stem cell
32	chr20:23731000-23732000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr20:23731200-23731400	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
34	chr20:23731400-23731600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
35	chr20:23731600-23733600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr20:23731800-23732000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr20:23731800-23732200	Enhancers	HUVEC	blood vessel
38	chr20:23732000-23732800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr20:23732200-23734200	Weak transcription	HUVEC	blood vessel
40	chr20:23732600-23734000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr20:23732800-23733200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr20:23733200-23733600	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr20:23733600-23737000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr20:23733800-23736600	Enhancers	NHDF-Ad	bronchial
45	chr20:23733800-23736800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr20:23734000-23736400	Enhancers	Muscle Satellite Cultured Cells	--
47	chr20:23734000-23736400	Enhancers	Osteobl	bone
48	chr20:23734000-23736800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr20:23734200-23734400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr20:23734200-23736600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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