Variant report

Variant	nsv458953
Chromosome Location	chr20:23731412-23808324
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	chr20:23747045-23747345	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
3	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
4	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
5	CEBPB	chr20:23786510-23786667	HepG2	liver:	n/a	chr20:23786550-23786561
6	CEBPB	chr20:23779809-23779920	HepG2	liver:	n/a	chr20:23779841-23779854
7	CTCF	chr20:23780000-23780150	GM12866	blood:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
8	CTCF	chr20:23779920-23780070	GM12870	blood:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
9	CTCF	chr20:23805840-23805990	SK-N-SH_RA	brain:	n/a	n/a
10	CTCF	chr20:23780240-23780390	GM12872	blood:	n/a	chr20:23780275-23780296 chr20:23780274-23780290 chr20:23780320-23780329 chr20:23780273-23780291
11	CTCF	chr20:23779800-23780070	GM12872	blood:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
12	CTCF	chr20:23763089-23763335	GM19240	blood:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
13	CTCF	chr20:23762700-23762850	WI-38	lung:	n/a	n/a
14	CTCF	chr20:23756740-23756890	HRE	kidney:	n/a	chr20:23756767-23756780
15	CTCF	chr20:23779880-23780030	HCFaa	heart:	n/a	n/a
16	CTCF	chr20:23763040-23763190	RPTEC	kidney:	n/a	n/a
17	CTCF	chr20:23763387-23763527	LNCaP	prostate:	n/a	chr20:23763450-23763471 chr20:23763448-23763466 chr20:23763449-23763465
18	CTCF	chr20:23780260-23780410	HRE	kidney:	n/a	chr20:23780275-23780296 chr20:23780274-23780290 chr20:23780320-23780329 chr20:23780273-23780291
19	CTCF	chr20:23779890-23780385	Fibrobl	skin:	n/a	chr20:23780275-23780296 chr20:23780274-23780290 chr20:23780320-23780329 chr20:23780273-23780291 chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
20	CTCF	chr20:23780249-23780347	GM12878	blood:	n/a	chr20:23780275-23780296 chr20:23780274-23780290 chr20:23780320-23780329 chr20:23780273-23780291
21	CTCF	chr20:23742005-23742067	Lung_OC	lung:	n/a	n/a
22	CTCF	chr20:23779960-23780110	GM12865	blood:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
23	CTCF	chr20:23780234-23780292	Medullo	brain:	n/a	chr20:23780274-23780290 chr20:23780273-23780291
24	CTCF	chr20:23779880-23780030	NHEK	skin:	n/a	n/a
25	CTCF	chr20:23763160-23763310	HCT-116	colon:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
26	CTCF	chr20:23779880-23780030	SAEC	small airway:	n/a	n/a
27	CTCF	chr20:23779833-23780212	GM12878	blood:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
28	CTCF	chr20:23780280-23780430	Caco-2	colon:	n/a	chr20:23780320-23780329
29	CTCF	chr20:23763080-23763230	GM12875	blood:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
30	CTCF	chr20:23779768-23780544	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
31	CTCF	chr20:23805983-23806110	LNCaP	prostate:	n/a	n/a
32	CTCF	chr20:23779880-23780030	HBMEC	blood vessel:	n/a	n/a
33	CTCF	chr20:23763039-23763574	MCF-7	breast:	n/a	chr20:23763450-23763471 chr20:23763448-23763466 chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210 chr20:23763449-23763465
34	CTCF	chr20:23763240-23763390	BE2_C	brain:	n/a	n/a
35	CTCF	chr20:23780360-23780510	GM12873	blood:	n/a	n/a
36	CTCF	chr20:23763060-23763486	A549	lung:	n/a	chr20:23763450-23763471 chr20:23763448-23763466 chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210 chr20:23763449-23763465
37	CTCF	chr20:23780280-23780430	HBMEC	blood vessel:	n/a	chr20:23780320-23780329
38	CTCF	chr20:23779880-23780030	Hela-S3	cervix:	n/a	n/a
39	CTCF	chr20:23779780-23780133	HCT-116	colon:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
40	CTCF	chr20:23805840-23805990	HEK293	kidney:	n/a	n/a
41	CTCF	chr20:23779960-23780110	AG04450	lung:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
42	CTCF	chr20:23780182-23780519	H1-hESC	embryonic stem cell:	n/a	chr20:23780275-23780296 chr20:23780274-23780290 chr20:23780320-23780329 chr20:23780273-23780291
43	CTCF	chr20:23800440-23800590	GM12864	blood:	n/a	n/a
44	CTCF	chr20:23763016-23763504	T-47D	breast:	n/a	chr20:23763450-23763471 chr20:23763448-23763466 chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210 chr20:23763449-23763465
45	CTCF	chr20:23779796-23780180	H1-hESC	embryonic stem cell:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
46	CTCF	chr20:23736040-23736190	HBMEC	blood vessel:	n/a	chr20:23736138-23736151
47	CTCF	chr20:23779880-23780030	AG10803	skin:	n/a	n/a
48	CTCF	chr20:23779980-23780130	GM12868	blood:	n/a	chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049
49	CTCF	chr20:23763034-23763588	HepG2	liver:	n/a	chr20:23763450-23763471 chr20:23763448-23763466 chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210 chr20:23763449-23763465
50	CTCF	chr20:23779876-23780421	A549	lung:	n/a	chr20:23780275-23780296 chr20:23780274-23780290 chr20:23780320-23780329 chr20:23780273-23780291 chr20:23780029-23780038 chr20:23780026-23780044 chr20:23780028-23780049

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:23731367-23731417	NH-A	brain:	n/a
2	chr20:23807359-23807409	Jurkat	blood:	n/a
3	chr20:23731367-23731417	NH-A	brain:	n/a
4	chr20:23807359-23807409	Jurkat	blood:	n/a
5	chr20:23807306-23807356	NHBE	bronchial:	n/a
6	chr20:23807359-23807409	HepG2	liver:	n/a
7	chr20:23806999-23807049	SAEC	small airway:	n/a
8	chr20:23807359-23807409	AG09309	skin:	n/a
9	chr20:23807359-23807409	GM06990	blood:	n/a
10	chr20:23807778-23807828	Hepatocyte	liver:	n/a
11	chr20:23732595-23732645	AG04449	skin:	fetal
12	chr20:23807359-23807409	ECC-1	luminal epithelium:	n/a
13	chr20:23807306-23807356	SK-N-SH_RA	brain:	n/a
14	chr20:23732873-23732923	NHDF-neo	bronchial:	n/a
15	chr20:23731367-23731417	SAEC	small airway:	n/a
16	chr20:23731367-23731417	GM19239	blood:	n/a
17	chr20:23732873-23732923	HCT-116	colon:	n/a
18	chr20:23731367-23731417	HIPEpiC	eye:	n/a
19	chr20:23807736-23807786	HCPEpiC	choroid plexus:	n/a
20	chr20:23807306-23807356	SK-N-SH	brain:	n/a
21	chr20:23807736-23807786	PANC-1	pancreas:	n/a
22	chr20:23806999-23807049	HNPCEpiC	eye:	n/a
23	chr20:23732595-23732645	BJ	skin:	n/a
24	chr20:23732595-23732645	HMEC	breast:	n/a
25	chr20:23807778-23807828	SK-N-SH	brain:	n/a
26	chr20:23731367-23731417	NHDF-neo	bronchial:	n/a
27	chr20:23807306-23807356	HEEpiC	esophagus:	n/a
28	chr20:23807736-23807786	NH-A	brain:	n/a
29	chr20:23806999-23807049	GM12878	blood:	n/a
30	chr20:23807736-23807786	RPTEC	kidney:	n/a
31	chr20:23732595-23732645	HUVEC	blood vessel:	n/a
32	chr20:23807778-23807828	Hela-S3	cervix:	n/a
33	chr20:23806999-23807049	SKMC	muscle:	n/a
34	chr20:23731367-23731417	HNPCEpiC	eye:	n/a
35	chr20:23807778-23807828	PANC-1	pancreas:	n/a
36	chr20:23807359-23807409	BJ	skin:	n/a
37	chr20:23807778-23807828	NHDF-neo	bronchial:	n/a
38	chr20:23806999-23807049	GM12892	blood:	n/a
39	chr20:23732595-23732645	PrEC	prostate:	n/a
40	chr20:23807778-23807828	PFSK-1	brain:	n/a
41	chr20:23731367-23731417	HEEpiC	esophagus:	n/a
42	chr20:23807778-23807828	K562	blood:	n/a
43	chr20:23807359-23807409	RPTEC	kidney:	n/a
44	chr20:23807736-23807786	HRE	kidney:	n/a
45	chr20:23732595-23732645	BE2_C	brain:	n/a
46	chr20:23807778-23807828	HRPEpiC	eye:	n/a
47	chr20:23807736-23807786	AG10803	skin:	n/a
48	chr20:23732873-23732923	GM12878	blood:	n/a
49	chr20:23732595-23732645	K562	blood:	n/a
50	chr20:23731367-23731417	ECC-1	luminal epithelium:	n/a

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

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

Variant related genes	Relation type
CST1	TF binding region
CST2	TF binding region
ENSG00000230908	TF binding region
CST1	CpG island
CST2	CpG island
ENSG00000230908	CpG island
XIAP	miRNA target sites
WWP2	miRNA target sites
WWC2	miRNA target sites

Extended variants
information (count: 2704 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:2704 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2070856	chr20:23731412-23731413	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs149367943	chr20:23731416-23731417	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs200307238	chr20:23731419-23731420	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs372905911	chr20:23731423-23731424	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs13045477	chr20:23731426-23731427	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
6	rs80263900	chr20:23731438-23731439	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs540721922	chr20:23731442-23731443	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs557370944	chr20:23731451-23731452	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs6076121	chr20:23731458-23731459	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs199758963	chr20:23731459-23731460	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs141813234	chr20:23731465-23731466	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs150586879	chr20:23731470-23731471	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs144543419	chr20:23731477-23731478	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs542879965	chr20:23731483-23731484	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs143142026	chr20:23731488-23731489	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs6076122	chr20:23731494-23731495	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs201315915	chr20:23731503-23731504	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs1141013	chr20:23731512-23731513	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs374004963	chr20:23731517-23731518	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs571670080	chr20:23731518-23731519	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs530782485	chr20:23731523-23731524	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs550064441	chr20:23731524-23731525	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs569886383	chr20:23731526-23731527	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs201376709	chr20:23731527-23731528	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs555186339	chr20:23731535-23731536	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs565527258	chr20:23731546-23731547	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs534420407	chr20:23731551-23731552	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs6076123	chr20:23731560-23731561	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs577584309	chr20:23731585-23731586	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs113896553	chr20:23731589-23731590	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
31	rs556897543	chr20:23731590-23731591	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs574300031	chr20:23731600-23731601	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs370685433	chr20:23731615-23731616	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs140676884	chr20:23731627-23731628	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs559999556	chr20:23731639-23731640	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs528650630	chr20:23731640-23731641	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs545539848	chr20:23731641-23731642	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs13045804	chr20:23731653-23731654	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs531019169	chr20:23731664-23731665	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs2070855	chr20:23731665-23731666	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs561328965	chr20:23731667-23731668	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs529213045	chr20:23731671-23731672	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs548823200	chr20:23731678-23731679	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs565562046	chr20:23731682-23731683	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs536277016	chr20:23731690-23731691	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs386813407	chr20:23731704-23731705	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs151261857	chr20:23731706-23731707	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs71333777	chr20:23731719-23731720	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs111818589	chr20:23731720-23731721	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs6083250	chr20:23731721-23731722	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	mRNA abundance

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:241 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:23726800-23731800	Weak transcription	HUVEC	blood vessel
2	chr20:23728800-23735000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr20:23729600-23734400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr20:23730800-23731600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr20:23731000-23732000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr20:23731400-23731600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
7	chr20:23731600-23733600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr20:23731800-23732000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr20:23731800-23732200	Enhancers	HUVEC	blood vessel
10	chr20:23732000-23732800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr20:23732200-23734200	Weak transcription	HUVEC	blood vessel
12	chr20:23732600-23734000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr20:23732800-23733200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr20:23733200-23733600	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr20:23733600-23737000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr20:23733800-23736600	Enhancers	NHDF-Ad	bronchial
17	chr20:23733800-23736800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr20:23734000-23736400	Enhancers	Muscle Satellite Cultured Cells	--
19	chr20:23734000-23736400	Enhancers	Osteobl	bone
20	chr20:23734000-23736800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr20:23734200-23734400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr20:23734200-23736600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr20:23734200-23737000	Enhancers	HUVEC	blood vessel
24	chr20:23734200-23737600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr20:23734400-23734600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr20:23734400-23735400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr20:23734400-23736400	Enhancers	HSMMtube	muscle
28	chr20:23734400-23736600	Enhancers	NHLF	lung
29	chr20:23734600-23735000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr20:23734600-23736200	Enhancers	HSMM	muscle
31	chr20:23735000-23737000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr20:23735000-23737200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr20:23735200-23736200	Enhancers	Left Ventricle	heart
34	chr20:23735200-23736600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr20:23735400-23735600	Bivalent Enhancer	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr20:23735400-23735800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr20:23735400-23736400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr20:23735400-23736400	Enhancers	Adipose Nuclei	Adipose
39	chr20:23735400-23736600	Enhancers	NH-A	brain
40	chr20:23735400-23737600	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
41	chr20:23735600-23735800	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
42	chr20:23735600-23736400	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
43	chr20:23735600-23736600	Enhancers	A549	lung
44	chr20:23735600-23737400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr20:23735800-23736000	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
46	chr20:23736000-23736200	Enhancers	Lung	lung
47	chr20:23736000-23736400	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
48	chr20:23736000-23737000	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr20:23736000-23737000	Enhancers	Gastric	stomach
50	chr20:23736200-23736400	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell

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