Variant report

Variant	esv3450213
Chromosome Location	chr20:23646333-23701687
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	chr20:23684405-23684588	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
4	CEBPB	chr20:23687946-23688194	A549	lung:	n/a	chr20:23688059-23688070
5	CEBPB	chr20:23687994-23688164	IMR90	lung:	n/a	chr20:23688059-23688070
6	CEBPB	chr20:23687909-23688202	HepG2	liver:	n/a	chr20:23688059-23688070
7	CEBPB	chr20:23655411-23655454	HepG2	liver:	n/a	n/a
8	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
9	CHD1	chr20:23648812-23649497	IMR90	lung:	n/a	n/a
10	CHD2	chr20:23649131-23649258	HepG2	liver:	n/a	n/a
11	CHD2	chr20:23649288-23649303	GM12878	blood:	n/a	n/a
12	CTCF	chr20:23646900-23647050	HFF	foreskin:	n/a	chr20:23646995-23647008 chr20:23646993-23647011 chr20:23646988-23647009
13	CTCF	chr20:23646960-23647110	AG09319	gingival:	n/a	chr20:23646995-23647008 chr20:23646993-23647011 chr20:23646988-23647009
14	CTCF	chr20:23649160-23649310	RPTEC	kidney:	n/a	chr20:23649201-23649222 chr20:23649199-23649217 chr20:23649200-23649216
15	CTCF	chr20:23646940-23647090	HPAF	blood vessel:	n/a	chr20:23646995-23647008 chr20:23646993-23647011 chr20:23646988-23647009
16	CTCF	chr20:23669495-23669583	Lung_OC	lung:	n/a	n/a
17	CTCF	chr20:23648878-23648993	GM19238	blood:	n/a	n/a
18	CTCF	chr20:23646940-23647090	HFF-Myc	foreskin:	n/a	chr20:23646995-23647008 chr20:23646993-23647011 chr20:23646988-23647009
19	CTCF	chr20:23650718-23650785	MCF-7	breast:	n/a	n/a
20	CTCF	chr20:23646952-23647072	GM12878	blood:	n/a	chr20:23646995-23647008 chr20:23646993-23647011 chr20:23646988-23647009
21	CTCF	chr20:23667740-23667890	HBMEC	blood vessel:	n/a	n/a
22	CTCF	chr20:23646940-23647090	NB4	blood:	n/a	chr20:23646995-23647008 chr20:23646993-23647011 chr20:23646988-23647009
23	CTCF	chr20:23648600-23648750	HVMF	connective:	n/a	n/a
24	CTCF	chr20:23649160-23649310	GM12868	blood:	n/a	chr20:23649200-23649216 chr20:23649201-23649222 chr20:23649199-23649217
25	CTCF	chr20:23649090-23649306	GM13976	blood:	n/a	chr20:23649201-23649222 chr20:23649199-23649217 chr20:23649200-23649216
26	CTCF	chr20:23668792-23668824	MCF-7	breast:	n/a	n/a
27	CTCF	chr20:23646940-23647090	AG10803	skin:	n/a	chr20:23646995-23647008 chr20:23646993-23647011 chr20:23646988-23647009
28	CTCF	chr20:23649140-23649290	GM12872	blood:	n/a	chr20:23649201-23649222 chr20:23649199-23649217 chr20:23649200-23649216
29	CTCF	chr20:23649140-23649290	HMEC	breast:	n/a	chr20:23649201-23649222 chr20:23649199-23649217 chr20:23649200-23649216
30	CTCF	chr20:23648916-23649713	A549	lung:	n/a	chr20:23649448-23649464 chr20:23649447-23649465 chr20:23649201-23649222 chr20:23649449-23649470 chr20:23649199-23649217 chr20:23649200-23649216
31	CTCF	chr20:23646920-23647070	SK-N-SH_RA	brain:	n/a	chr20:23646995-23647008 chr20:23646993-23647011 chr20:23646988-23647009
32	CTCF	chr20:23646960-23647110	K562	blood:	n/a	chr20:23646995-23647008 chr20:23646993-23647011 chr20:23646988-23647009
33	CTCF	chr20:23649140-23649290	GM12865	blood:	n/a	chr20:23649201-23649222 chr20:23649199-23649217 chr20:23649200-23649216
34	CTCF	chr20:23646900-23647050	AG04450	lung:	n/a	chr20:23646995-23647008 chr20:23646993-23647011 chr20:23646988-23647009
35	CTCF	chr20:23649160-23649310	NHEK	skin:	n/a	chr20:23649201-23649222 chr20:23649199-23649217 chr20:23649200-23649216
36	CTCF	chr20:23649061-23649568	T-47D	breast:	n/a	chr20:23649448-23649464 chr20:23649447-23649465 chr20:23649201-23649222 chr20:23649449-23649470 chr20:23649199-23649217 chr20:23649200-23649216
37	CTCF	chr20:23646960-23647110	GM12864	blood:	n/a	chr20:23646995-23647008 chr20:23646993-23647011 chr20:23646988-23647009
38	CTCF	chr20:23646940-23647090	AG04449	skin:	n/a	chr20:23646995-23647008 chr20:23646993-23647011 chr20:23646988-23647009
39	CTCF	chr20:23649057-23649344	GM19239	blood:	n/a	chr20:23649201-23649222 chr20:23649199-23649217 chr20:23649200-23649216
40	CTCF	chr20:23646920-23647070	MCF-7	breast:	n/a	chr20:23646995-23647008 chr20:23646993-23647011 chr20:23646988-23647009
41	CTCF	chr20:23649120-23649270	HCM	heart:	n/a	chr20:23649201-23649222 chr20:23649199-23649217 chr20:23649200-23649216
42	CTCF	chr20:23649160-23649310	BJ	skin:	n/a	chr20:23649201-23649222 chr20:23649199-23649217 chr20:23649200-23649216
43	CTCF	chr20:23648280-23648430	GM12874	blood:	n/a	n/a
44	CTCF	chr20:23648974-23649651	MCF-7	breast:	n/a	chr20:23649448-23649464 chr20:23649447-23649465 chr20:23649201-23649222 chr20:23649449-23649470 chr20:23649199-23649217 chr20:23649200-23649216
45	CTCF	chr20:23649070-23649585	MCF-7	breast:	n/a	chr20:23649448-23649464 chr20:23649447-23649465 chr20:23649201-23649222 chr20:23649449-23649470 chr20:23649199-23649217 chr20:23649200-23649216
46	CTCF	chr20:23649160-23649310	HCT-116	colon:	n/a	chr20:23649201-23649222 chr20:23649199-23649217 chr20:23649200-23649216
47	CTCF	chr20:23649009-23649586	HepG2	liver:	n/a	chr20:23649448-23649464 chr20:23649447-23649465 chr20:23649201-23649222 chr20:23649449-23649470 chr20:23649199-23649217 chr20:23649200-23649216
48	CTCF	chr20:23649566-23649570	HepG2	liver:	n/a	n/a
49	CTCF	chr20:23660067-23660083	MCF-7	breast:	n/a	n/a
50	CTCF	chr20:23649065-23649552	NHEK	skin:	n/a	chr20:23649448-23649464 chr20:23649447-23649465 chr20:23649201-23649222 chr20:23649449-23649470 chr20:23649199-23649217 chr20:23649200-23649216

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:23669470-23669520	GM12891	blood:	n/a
2	chr20:23670047-23670097	HPAEpiC	pulmonary alveolar:	n/a
3	chr20:23670047-23670097	U87	brain:	n/a
4	chr20:23670047-23670097	K562	blood:	n/a
5	chr20:23671108-23671158	HRE	kidney:	n/a
6	chr20:23670047-23670097	AG04449	skin:	fetal
7	chr20:23669241-23669291	CMK	blood:	n/a
8	chr20:23671108-23671158	SAEC	small airway:	n/a
9	chr20:23671108-23671158	K562	blood:	n/a
10	chr20:23670089-23670139	NH-A	brain:	n/a
11	chr20:23669470-23669520	HEK293	kidney:	embryo
12	chr20:23670047-23670097	AG10803	skin:	n/a
13	chr20:23669241-23669291	K562	blood:	n/a
14	chr20:23670089-23670139	HCT-116	colon:	n/a
15	chr20:23669470-23669520	GM12892	blood:	n/a
16	chr20:23670089-23670139	MCF-7	breast:	n/a
17	chr20:23669241-23669291	H1-hESC	embryonic stem cell:	embryo
18	chr20:23669241-23669291	U87	brain:	n/a
19	chr20:23670047-23670097	PANC-1	pancreas:	n/a
20	chr20:23666505-23666555	HCF	heart:	n/a
21	chr20:23670047-23670097	Caco-2	colon:	n/a
22	chr20:23669470-23669520	SKMC	muscle:	n/a
23	chr20:23669470-23669520	SK-N-SH_RA	brain:	n/a
24	chr20:23669241-23669291	ECC-1	luminal epithelium:	n/a
25	chr20:23669470-23669520	HPAEpiC	pulmonary alveolar:	n/a
26	chr20:23670047-23670097	HCM	heart:	n/a
27	chr20:23670089-23670139	GM06990	blood:	n/a
28	chr20:23670089-23670139	PFSK-1	brain:	n/a
29	chr20:23670047-23670097	RPTEC	kidney:	n/a
30	chr20:23670047-23670097	GM12891	blood:	n/a
31	chr20:23666505-23666555	HNPCEpiC	eye:	n/a
32	chr20:23670089-23670139	Hela-S3	cervix:	n/a
33	chr20:23670047-23670097	CMK	blood:	n/a
34	chr20:23670089-23670139	HepG2	liver:	n/a
35	chr20:23670047-23670097	HCT-116	colon:	n/a
36	chr20:23670047-23670097	HCF	heart:	n/a
37	chr20:23670047-23670097	NHDF-neo	bronchial:	n/a
38	chr20:23670047-23670097	AG09309	skin:	n/a
39	chr20:23666505-23666555	SK-N-MC	brain:	n/a
40	chr20:23670047-23670097	BE2_C	brain:	n/a
41	chr20:23671108-23671158	ovcar-3	ovarian:	n/a
42	chr20:23671108-23671158	GM12892	blood:	n/a
43	chr20:23670047-23670097	BJ	skin:	n/a
44	chr20:23666505-23666555	ECC-1	luminal epithelium:	n/a
45	chr20:23669470-23669520	HMEC	breast:	n/a
46	chr20:23669470-23669520	BE2_C	brain:	n/a
47	chr20:23669241-23669291	LNCaP	prostate:	n/a
48	chr20:23666505-23666555	NH-A	brain:	n/a
49	chr20:23669241-23669291	HUVEC	blood vessel:	n/a
50	chr20:23669241-23669291	SK-N-SH_RA	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr20:23648767..23649721-chr20:23779902..23780425,2	MCF-7	breast:
2	chr20:23648920..23650143-chr20:23704363..23705222,5	MCF-7	breast:
3	chr20:23648954..23649672-chr20:23703387..23704074,2	MCF-7	breast:
4	chr20:23648334..23649447-chr20:23704109..23705001,3	MCF-7	breast:
5	chr20:23648842..23649774-chr20:23870335..23871266,4	MCF-7	breast:
6	chr20:23648665..23649293-chr20:23837547..23838405,2	MCF-7	breast:
7	chr20:23649188..23649689-chr20:23762769..23763504,2	MCF-7	breast:
8	chr20:23649611..23652412-chr20:23660454..23663208,2	MCF-7	breast:
9	chr20:23649611..23652412-chr20:23660454..23663208,2	MCF-7	breast:

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

Extended variants
information (count: 2326 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:2326 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs183697853	chr20:23646345-23646346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs559263414	chr20:23646421-23646422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs536248962	chr20:23646467-23646468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs553355228	chr20:23646477-23646478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs116093642	chr20:23646486-23646487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs571982890	chr20:23646497-23646498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs367653362	chr20:23646528-23646529	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs536007303	chr20:23646553-23646554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs150742347	chr20:23646555-23646556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs201698380	chr20:23646616-23646617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs139118183	chr20:23646630-23646631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs554696799	chr20:23646659-23646660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs187976954	chr20:23646687-23646688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs371880396	chr20:23646721-23646722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs544760358	chr20:23646781-23646782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs190547985	chr20:23646782-23646783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs149905646	chr20:23646793-23646794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs2424597	chr20:23646809-23646810	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs183154603	chr20:23646828-23646829	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs528417320	chr20:23646839-23646840	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs140519357	chr20:23646840-23646841	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs144485785	chr20:23646844-23646845	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs530518585	chr20:23646862-23646863	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs187125426	chr20:23646891-23646892	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs6138031	chr20:23646900-23646901	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs191943262	chr20:23646970-23646971	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs577078530	chr20:23646991-23646992	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs373560783	chr20:23646994-23646995	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs147857144	chr20:23646996-23646997	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs141529853	chr20:23647002-23647003	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs539381288	chr20:23647005-23647006	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs559190184	chr20:23647007-23647008	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs575858789	chr20:23647040-23647041	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs184902208	chr20:23647059-23647060	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs142836621	chr20:23647091-23647092	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs574901337	chr20:23647099-23647100	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs151063131	chr20:23647119-23647120	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs187467444	chr20:23647163-23647164	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs115648483	chr20:23647241-23647242	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs559517271	chr20:23647251-23647252	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs192750765	chr20:23647330-23647331	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs570787313	chr20:23647335-23647336	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs140966379	chr20:23647346-23647347	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs530580263	chr20:23647370-23647371	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs150221833	chr20:23647413-23647414	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs537967102	chr20:23647426-23647427	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs16997177	chr20:23647429-23647430	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs201211348	chr20:23647433-23647434	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs1884861	chr20:23647482-23647483	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs546268750	chr20:23647484-23647485	Weak transcription Enhancers Bivalent Enhancer	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
Gastric cancer	22014070	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:200 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:23637200-23660000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr20:23641800-23647000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr20:23641800-23647200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr20:23641800-23647200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr20:23641800-23652200	Weak transcription	Adipose Nuclei	Adipose
6	chr20:23642400-23649400	Weak transcription	Skeletal Muscle Male	skeletal muscle
7	chr20:23642600-23647000	Weak transcription	Primary monocytes fromperipheralblood	blood
8	chr20:23642600-23647000	Weak transcription	Monocytes-CD14+_RO01746	blood
9	chr20:23643400-23646800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr20:23643800-23647800	Weak transcription	Fetal Muscle Leg	muscle
11	chr20:23644000-23648400	Weak transcription	Fetal Muscle Trunk	muscle
12	chr20:23645800-23647000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr20:23646000-23647000	Weak transcription	Spleen	Spleen
14	chr20:23646000-23649200	Weak transcription	HepG2	liver
15	chr20:23646800-23647200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr20:23647000-23647200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr20:23647000-23647600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr20:23647000-23647600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr20:23647000-23647600	Enhancers	Monocytes-CD14+_RO01746	blood
20	chr20:23647000-23647800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr20:23647000-23648000	Enhancers	Primary monocytes fromperipheralblood	blood
22	chr20:23647000-23648000	Enhancers	Cortex derived primary cultured neurospheres	brain
23	chr20:23647000-23648000	Enhancers	HUVEC	blood vessel
24	chr20:23647000-23648200	Enhancers	Spleen	Spleen
25	chr20:23647000-23648800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
26	chr20:23647200-23647400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr20:23647200-23648000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr20:23647200-23648400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr20:23647400-23648000	Enhancers	HSMMtube	muscle
30	chr20:23647400-23648200	Enhancers	Fetal Lung	lung
31	chr20:23647600-23648600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr20:23647800-23648200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr20:23647800-23648200	Enhancers	Fetal Muscle Leg	muscle
34	chr20:23647800-23648200	Weak transcription	Skeletal Muscle Female	skeletal muscle
35	chr20:23648200-23648400	Weak transcription	Fetal Muscle Leg	muscle
36	chr20:23648200-23648400	Enhancers	Skeletal Muscle Female	skeletal muscle
37	chr20:23648200-23649400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr20:23648200-23650400	Weak transcription	Spleen	Spleen
39	chr20:23648400-23648600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr20:23648400-23648600	Enhancers	Fetal Muscle Trunk	muscle
41	chr20:23648400-23648800	Enhancers	Fetal Muscle Leg	muscle
42	chr20:23648400-23649200	Weak transcription	Skeletal Muscle Female	skeletal muscle
43	chr20:23648600-23648800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr20:23648600-23649000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr20:23648800-23649200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr20:23649000-23650400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr20:23649200-23649400	Enhancers	Skeletal Muscle Female	skeletal muscle
48	chr20:23649200-23649600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr20:23649200-23649600	Enhancers	HepG2	liver
50	chr20:23649400-23649600	Enhancers	Skeletal Muscle Male	skeletal muscle

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