Variant report

Variant	esv3454909
Chromosome Location	chr20:23643949-23775044
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	ARID3A	chr20:23649147-23649450	HepG2	liver:	n/a	n/a
2	BRCA1	chr20:23649179-23649335	HepG2	liver:	n/a	n/a
3	CEBPB	chr20:23715126-23715326	A549	lung:	n/a	chr20:23715271-23715282
4	CEBPB	chr20:23687994-23688164	IMR90	lung:	n/a	chr20:23688059-23688070
5	CEBPB	chr20:23687909-23688202	HepG2	liver:	n/a	chr20:23688059-23688070
6	CEBPB	chr20:23710603-23710866	H1-hESC	embryonic stem cell:	n/a	chr20:23710701-23710712
7	CEBPB	chr20:23684500-23684595	A549	lung:	n/a	chr20:23684504-23684515 chr20:23684504-23684517 chr20:23684506-23684515 chr20:23684506-23684515 chr20:23684506-23684515 chr20:23684506-23684517 chr20:23684506-23684515
8	CEBPB	chr20:23710540-23710875	HepG2	liver:	n/a	chr20:23710701-23710712
9	CEBPB	chr20:23715136-23715338	IMR90	lung:	n/a	chr20:23715271-23715282
10	CEBPB	chr20:23684405-23684588	HepG2	liver:	n/a	chr20:23684504-23684515 chr20:23684504-23684517 chr20:23684506-23684515 chr20:23684506-23684515 chr20:23684506-23684515 chr20:23684506-23684517 chr20:23684506-23684515
11	CEBPB	chr20:23715133-23715386	HepG2	liver:	n/a	chr20:23715271-23715282
12	CEBPB	chr20:23710550-23710870	IMR90	lung:	n/a	chr20:23710701-23710712
13	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
14	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
15	CEBPB	chr20:23710539-23710875	A549	lung:	n/a	chr20:23710701-23710712
16	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
17	CEBPB	chr20:23655411-23655454	HepG2	liver:	n/a	n/a
18	CEBPB	chr20:23710656-23710785	K562	blood:	n/a	chr20:23710701-23710712
19	CEBPB	chr20:23687946-23688194	A549	lung:	n/a	chr20:23688059-23688070
20	CHD1	chr20:23648812-23649497	IMR90	lung:	n/a	n/a
21	CHD2	chr20:23649131-23649258	HepG2	liver:	n/a	n/a
22	CHD2	chr20:23649288-23649303	GM12878	blood:	n/a	n/a
23	CHD2	chr20:23643986-23644012	HepG2	liver:	n/a	n/a
24	CTCF	chr20:23731080-23731230	GM12871	blood:	n/a	n/a
25	CTCF	chr20:23704350-23704970	K562	blood:	n/a	chr20:23704495-23704516 chr20:23704493-23704511 chr20:23704741-23704757 chr20:23704742-23704763 chr20:23704496-23704505 chr20:23704787-23704796 chr20:23704740-23704758
26	CTCF	chr20:23763160-23763310	HCT-116	colon:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
27	CTCF	chr20:23648280-23648430	GM12874	blood:	n/a	n/a
28	CTCF	chr20:23646960-23647110	AG04449	skin:	n/a	chr20:23646995-23647008 chr20:23646993-23647011 chr20:23646988-23647009
29	CTCF	chr20:23729680-23729830	GM12866	blood:	n/a	n/a
30	CTCF	chr20:23649120-23649270	HEEpiC	esophagus:	n/a	chr20:23649201-23649222 chr20:23649199-23649217 chr20:23649200-23649216
31	CTCF	chr20:23649077-23649323	H1-hESC	embryonic stem cell:	n/a	chr20:23649201-23649222 chr20:23649199-23649217 chr20:23649200-23649216
32	CTCF	chr20:23646994-23647023	Fibrobl	skin:	n/a	chr20:23646995-23647008
33	CTCF	chr20:23756746-23756816	K562	blood:	n/a	chr20:23756767-23756780
34	CTCF	chr20:23763220-23763370	NHLF	lung:	n/a	n/a
35	CTCF	chr20:23649140-23649290	HCFaa	heart:	n/a	chr20:23649201-23649222 chr20:23649199-23649217 chr20:23649200-23649216
36	CTCF	chr20:23646920-23647070	BJ	skin:	n/a	chr20:23646995-23647008 chr20:23646993-23647011 chr20:23646988-23647009
37	CTCF	chr20:23649140-23649290	AG04450	lung:	n/a	chr20:23649201-23649222 chr20:23649199-23649217 chr20:23649200-23649216
38	CTCF	chr20:23648986-23649573	GM12878	blood:	n/a	chr20:23649448-23649464 chr20:23649447-23649465 chr20:23649201-23649222 chr20:23649449-23649470 chr20:23649199-23649217 chr20:23649200-23649216
39	CTCF	chr20:23704350-23704892	MCF-7	breast:	n/a	chr20:23704495-23704516 chr20:23704493-23704511 chr20:23704741-23704757 chr20:23704742-23704763 chr20:23704496-23704505 chr20:23704787-23704796 chr20:23704740-23704758
40	CTCF	chr20:23763074-23763319	GM13977	blood:	n/a	chr20:23763195-23763204 chr20:23763194-23763215 chr20:23763192-23763210
41	CTCF	chr20:23704060-23704210	MCF-7	breast:	n/a	n/a
42	CTCF	chr20:23729741-23729801	GM19239	blood:	n/a	n/a
43	CTCF	chr20:23704280-23704430	NHDF-neo	bronchial:	n/a	n/a
44	CTCF	chr20:23704420-23704570	GM12872	blood:	n/a	chr20:23704495-23704516 chr20:23704493-23704511 chr20:23704496-23704505
45	CTCF	chr20:23646880-23647030	Hela-S3	cervix:	n/a	chr20:23646995-23647008 chr20:23646993-23647011 chr20:23646988-23647009
46	CTCF	chr20:23672360-23672510	WERI-Rb-1	eye:	n/a	n/a
47	CTCF	chr20:23646920-23647070	AoAF	blood vessel:	n/a	chr20:23646995-23647008 chr20:23646993-23647011 chr20:23646988-23647009
48	CTCF	chr20:23756580-23756730	HA-sp	spinal cord:	n/a	n/a
49	CTCF	chr20:23763020-23763170	RPTEC	kidney:	n/a	n/a
50	CTCF	chr20:23667860-23668010	WERI-Rb-1	eye:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:23671108-23671158	NB4	blood:	n/a
2	chr20:23670089-23670139	NHDF-neo	bronchial:	n/a
3	chr20:23671108-23671158	H1-hESC	embryonic stem cell:	embryo
4	chr20:23671108-23671158	HAEpiC	amniotic membrane:	n/a
5	chr20:23732873-23732923	BJ	skin:	n/a
6	chr20:23728814-23728864	A549	lung:	n/a
7	chr20:23670089-23670139	HRCEpiC	kidney:	n/a
8	chr20:23669241-23669291	PFSK-1	brain:	n/a
9	chr20:23728432-23728482	HNPCEpiC	eye:	n/a
10	chr20:23671108-23671158	BJ	skin:	n/a
11	chr20:23669470-23669520	ProgFib	skin:	n/a
12	chr20:23731367-23731417	ProgFib	skin:	n/a
13	chr20:23732873-23732923	HL-60	blood:	n/a
14	chr20:23731367-23731417	HMEC	breast:	n/a
15	chr20:23732873-23732923	ProgFib	skin:	n/a
16	chr20:23669241-23669291	MCF-7	breast:	n/a
17	chr20:23669470-23669520	SK-N-MC	brain:	n/a
18	chr20:23728432-23728482	HCPEpiC	choroid plexus:	n/a
19	chr20:23728814-23728864	HEEpiC	esophagus:	n/a
20	chr20:23731367-23731417	Jurkat	blood:	n/a
21	chr20:23732595-23732645	U87	brain:	n/a
22	chr20:23731367-23731417	SKMC	muscle:	n/a
23	chr20:23731367-23731417	NHDF-neo	bronchial:	n/a
24	chr20:23732595-23732645	AG10803	skin:	n/a
25	chr20:23669470-23669520	GM06990	blood:	n/a
26	chr20:23669470-23669520	AG10803	skin:	n/a
27	chr20:23670089-23670139	HCPEpiC	choroid plexus:	n/a
28	chr20:23670047-23670097	Hela-S3	cervix:	n/a
29	chr20:23728432-23728482	HCF	heart:	n/a
30	chr20:23732873-23732923	CMK	blood:	n/a
31	chr20:23728432-23728482	HAEpiC	amniotic membrane:	n/a
32	chr20:23670047-23670097	AG04450	lung:	fetal
33	chr20:23666505-23666555	Jurkat	blood:	n/a
34	chr20:23732873-23732923	AG09319	gingival:	n/a
35	chr20:23670089-23670139	K562	blood:	n/a
36	chr20:23670047-23670097	BE2_C	brain:	n/a
37	chr20:23670047-23670097	Hepatocyte	liver:	n/a
38	chr20:23728814-23728864	AG09319	gingival:	n/a
39	chr20:23732595-23732645	Caco-2	colon:	n/a
40	chr20:23666505-23666555	ProgFib	skin:	n/a
41	chr20:23728432-23728482	BE2_C	brain:	n/a
42	chr20:23732873-23732923	HEK293	kidney:	embryo
43	chr20:23732595-23732645	A549	lung:	n/a
44	chr20:23666505-23666555	NHBE	bronchial:	n/a
45	chr20:23669241-23669291	HIPEpiC	eye:	n/a
46	chr20:23669241-23669291	AG04449	skin:	fetal
47	chr20:23732595-23732645	HRE	kidney:	n/a
48	chr20:23732595-23732645	MCF-7	breast:	n/a
49	chr20:23728432-23728482	GM12878	blood:	n/a
50	chr20:23732873-23732923	NHDF-neo	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr20:23645187..23645712-chr20:23775888..23776677,2	MCF-7	breast:
2	chr20:23648665..23649293-chr20:23837547..23838405,2	MCF-7	breast:
3	chr20:23704490..23705249-chr20:23762654..23763235,2	MCF-7	breast:
4	chr20:23648334..23649447-chr20:23704109..23705001,3	MCF-7	breast:
5	chr20:23702805..23703439-chr20:23754485..23755364,2	MCF-7	breast:
6	chr20:23702805..23703439-chr20:23754485..23755364,2	MCF-7	breast:
7	chr20:23648954..23649672-chr20:23703387..23704074,2	MCF-7	breast:
8	chr20:23704491..23705478-chr20:23779622..23780975,4	MCF-7	breast:
9	chr20:23648334..23649447-chr20:23704109..23705001,3	MCF-7	breast:
10	chr20:23649611..23652412-chr20:23660454..23663208,2	MCF-7	breast:
11	chr20:23704352..23705295-chr20:23754423..23755304,4	MCF-7	breast:
12	chr20:23649188..23649689-chr20:23762769..23763504,2	MCF-7	breast:
13	chr20:23763057..23763763-chr20:23870036..23871243,3	MCF-7	breast:
14	chr20:23754506..23755505-chr20:23837367..23838288,3	MCF-7	breast:
15	chr20:23648920..23650143-chr20:23704363..23705222,5	MCF-7	breast:
16	chr20:23649611..23652412-chr20:23660454..23663208,2	MCF-7	breast:
17	chr20:23648954..23649672-chr20:23703387..23704074,2	MCF-7	breast:
18	chr20:23704352..23705295-chr20:23754423..23755304,4	MCF-7	breast:
19	chr20:23648842..23649774-chr20:23870335..23871266,4	MCF-7	breast:
20	chr20:23649188..23649689-chr20:23762769..23763504,2	MCF-7	breast:
21	chr20:23704490..23705249-chr20:23762654..23763235,2	MCF-7	breast:
22	chr20:23648767..23649721-chr20:23779902..23780425,2	MCF-7	breast:
23	chr20:23648920..23650143-chr20:23704363..23705222,5	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CST8-5	chr20:23732376-23732473	NONHSAT079083
2	lnc-CST8-5	chr20:23733160-23733281	NONHSAT079083
3	lnc-CST8-5	chr20:23726778-23726924	NONHSAT079083
4	lnc-CST8-5	chr20:23733871-23734300	NONHSAT079083

Variant related genes	Relation type
CST4	TF binding region
CST2P1	TF binding region
ENSG00000230908	TF binding region
CST1	TF binding region
CST4	CpG island
CST2P1	CpG island
ENSG00000230908	CpG island
CST1	CpG island

Extended variants
information (count: 5132 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:5132 , 50 per page) page: 1 2 3 4 5 6 7 ... 103

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs140203853	chr20:23643984-23643985	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs570906840	chr20:23644028-23644029	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs192223912	chr20:23644032-23644033	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs555329823	chr20:23644049-23644050	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs142351861	chr20:23644050-23644051	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs201784594	chr20:23644074-23644075	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs368063175	chr20:23644094-23644095	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs73318188	chr20:23644106-23644107	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs373738097	chr20:23644111-23644112	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs367579180	chr20:23644128-23644129	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs372316916	chr20:23644132-23644133	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs116712799	chr20:23644152-23644153	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs577080682	chr20:23644154-23644155	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs545993250	chr20:23644162-23644163	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs556422036	chr20:23644163-23644164	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs576190911	chr20:23644166-23644167	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs188785706	chr20:23644215-23644216	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs561630887	chr20:23644255-23644256	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs527243059	chr20:23644263-23644264	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs113748002	chr20:23644272-23644273	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs540685561	chr20:23644345-23644346	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs542689119	chr20:23644373-23644374	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs2424595	chr20:23644387-23644388	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs533481540	chr20:23644405-23644406	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs151009305	chr20:23644414-23644415	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs569954358	chr20:23644438-23644439	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs529345532	chr20:23644492-23644493	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs557625432	chr20:23644494-23644495	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs549021784	chr20:23644518-23644519	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs566053143	chr20:23644526-23644527	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs34599074	chr20:23644531-23644532	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs534984952	chr20:23644586-23644587	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs576299162	chr20:23644590-23644591	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs557889414	chr20:23644622-23644623	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs570703692	chr20:23644658-23644659	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs11905347	chr20:23644659-23644660	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs556385320	chr20:23644661-23644662	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs184515799	chr20:23644673-23644674	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs190628832	chr20:23644688-23644689	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs543783014	chr20:23644704-23644705	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs181931538	chr20:23644711-23644712	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs377217498	chr20:23644764-23644765	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs142223315	chr20:23644785-23644786	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs540996928	chr20:23644790-23644791	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs565189694	chr20:23644808-23644809	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs187434408	chr20:23644881-23644882	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs563958252	chr20:23644892-23644893	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs188813914	chr20:23644894-23644895	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs543751350	chr20:23644900-23644901	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs563644253	chr20:23644918-23644919	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

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
Gastric cancer	22014070	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:419 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:23637200-23660000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr20:23637800-23644200	Enhancers	Fetal Intestine Large	intestine
3	chr20:23638400-23644200	Enhancers	Fetal Intestine Small	intestine
4	chr20:23641800-23647000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr20:23641800-23647200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr20:23641800-23647200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr20:23641800-23652200	Weak transcription	Adipose Nuclei	Adipose
8	chr20:23642400-23644800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr20:23642400-23649400	Weak transcription	Skeletal Muscle Male	skeletal muscle
10	chr20:23642600-23647000	Weak transcription	Primary monocytes fromperipheralblood	blood
11	chr20:23642600-23647000	Weak transcription	Monocytes-CD14+_RO01746	blood
12	chr20:23643000-23644000	Enhancers	Fetal Muscle Trunk	muscle
13	chr20:23643200-23644200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr20:23643200-23646000	Enhancers	HepG2	liver
15	chr20:23643400-23646800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr20:23643800-23647800	Weak transcription	Fetal Muscle Leg	muscle
17	chr20:23644000-23644200	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr20:23644000-23648400	Weak transcription	Fetal Muscle Trunk	muscle
19	chr20:23644800-23645000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr20:23644800-23645400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr20:23645000-23645600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr20:23645400-23646200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr20:23645600-23645800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr20:23645800-23646000	Enhancers	Spleen	Spleen
25	chr20:23645800-23647000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr20:23646000-23647000	Weak transcription	Spleen	Spleen
27	chr20:23646000-23649200	Weak transcription	HepG2	liver
28	chr20:23646800-23647200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr20:23647000-23647200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr20:23647000-23647600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr20:23647000-23647600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr20:23647000-23647600	Enhancers	Monocytes-CD14+_RO01746	blood
33	chr20:23647000-23647800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr20:23647000-23648000	Enhancers	Primary monocytes fromperipheralblood	blood
35	chr20:23647000-23648000	Enhancers	Cortex derived primary cultured neurospheres	brain
36	chr20:23647000-23648000	Enhancers	HUVEC	blood vessel
37	chr20:23647000-23648200	Enhancers	Spleen	Spleen
38	chr20:23647000-23648800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
39	chr20:23647200-23647400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr20:23647200-23648000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr20:23647200-23648400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr20:23647400-23648000	Enhancers	HSMMtube	muscle
43	chr20:23647400-23648200	Enhancers	Fetal Lung	lung
44	chr20:23647600-23648600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr20:23647800-23648200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr20:23647800-23648200	Enhancers	Fetal Muscle Leg	muscle
47	chr20:23647800-23648200	Weak transcription	Skeletal Muscle Female	skeletal muscle
48	chr20:23648200-23648400	Weak transcription	Fetal Muscle Leg	muscle
49	chr20:23648200-23648400	Enhancers	Skeletal Muscle Female	skeletal muscle
50	chr20:23648200-23649400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin

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