Variant report

Variant	esv2758801
Chromosome Location	chr20:52679137-52685208
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:576)
CpG islands
(count:0)
Chromatin interactive
region (count:92)
LncRNA
region (count:0)
Mature miRNA
region (count: 2)
miRNA target
sites (count:0)

(count:576 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr20:52679243-52679598	K562	blood:	n/a	n/a
2	ARID3A	chr20:52679309-52679659	HepG2	liver:	n/a	n/a
3	ARID3A	chr20:52683823-52684558	HepG2	liver:	n/a	n/a
4	ARID3A	chr20:52682222-52682596	K562	blood:	n/a	n/a
5	ATF1	chr20:52682154-52682556	K562	blood:	n/a	n/a
6	ATF2	chr20:52680440-52680905	GM12878	blood:	n/a	n/a
7	ATF2	chr20:52680343-52681175	GM12878	blood:	n/a	n/a
8	ATF3	chr20:52684073-52684687	A549	lung:	n/a	n/a
9	ATF3	chr20:52683947-52684750	A549	lung:	n/a	n/a
10	BATF	chr20:52684188-52684426	GM12878	blood:	n/a	chr20:52684257-52684265
11	BATF	chr20:52684107-52684494	GM12878	blood:	n/a	chr20:52684257-52684265
12	BATF	chr20:52680433-52681023	GM12878	blood:	n/a	n/a
13	BCL11A	chr20:52680494-52680861	GM12878	blood:	n/a	n/a
14	BCL3	chr20:52684032-52684751	A549	lung:	n/a	n/a
15	BCL3	chr20:52683878-52684754	A549	lung:	n/a	n/a
16	BCLAF1	chr20:52679262-52679665	GM12878	blood:	n/a	n/a
17	BHLHE40	chr20:52679314-52679587	K562	blood:	n/a	n/a
18	BHLHE40	chr20:52684148-52684627	HepG2	liver:	n/a	n/a
19	BHLHE40	chr20:52680387-52681544	GM12878	blood:	n/a	n/a
20	BHLHE40	chr20:52681921-52682597	K562	blood:	n/a	n/a
21	BRCA1	chr20:52679785-52679787	HepG2	liver:	n/a	n/a
22	BRCA1	chr20:52684039-52684672	Hela-S3	cervix:	n/a	n/a
23	BRCA1	chr20:52684322-52684471	HepG2	liver:	n/a	n/a
24	CBX3	chr20:52682226-52682598	K562	blood:	n/a	n/a
25	CBX3	chr20:52682063-52682605	K562	blood:	n/a	n/a
26	CBX3	chr20:52683997-52684770	HCT-116	colon:	n/a	n/a
27	CCNT2	chr20:52682120-52682619	K562	blood:	n/a	chr20:52682440-52682460
28	CEBPB	chr20:52684171-52684522	HepG2	liver:	n/a	n/a
29	CEBPB	chr20:52684060-52684576	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr20:52684129-52684584	A549	lung:	n/a	n/a
31	CEBPB	chr20:52683921-52684823	HCT-116	colon:	n/a	n/a
32	CEBPB	chr20:52682158-52682566	K562	blood:	n/a	n/a
33	CEBPB	chr20:52684238-52684470	HepG2	liver:	n/a	n/a
34	CEBPB	chr20:52679318-52679687	A549	lung:	n/a	chr20:52679565-52679578 chr20:52679565-52679576 chr20:52679566-52679577
35	CEBPB	chr20:52683964-52684941	A549	lung:	n/a	n/a
36	CEBPB	chr20:52682049-52682578	K562	blood:	n/a	n/a
37	CEBPB	chr20:52679438-52679701	HepG2	liver:	n/a	chr20:52679565-52679578 chr20:52679565-52679576 chr20:52679566-52679577
38	CEBPB	chr20:52684171-52684490	A549	lung:	n/a	n/a
39	CEBPD	chr20:52682189-52682660	K562	blood:	n/a	n/a
40	CEBPD	chr20:52684125-52684590	HepG2	liver:	n/a	n/a
41	CEBPD	chr20:52681445-52682008	K562	blood:	n/a	n/a
42	CEBPD	chr20:52682116-52682652	K562	blood:	n/a	n/a
43	CHD2	chr20:52680383-52681324	GM12878	blood:	n/a	n/a
44	CHD2	chr20:52684103-52684614	HepG2	liver:	n/a	n/a
45	CHD2	chr20:52684089-52684613	Hela-S3	cervix:	n/a	n/a
46	CREB1	chr20:52682073-52682709	K562	blood:	n/a	n/a
47	CREB1	chr20:52684157-52684486	A549	lung:	n/a	n/a
48	CREB1	chr20:52684171-52684577	A549	lung:	n/a	n/a
49	CTCF	chr20:52679400-52679550	GM12865	blood:	n/a	chr20:52679464-52679485 chr20:52679469-52679487 chr20:52679470-52679486
50	CTCF	chr20:52679337-52679581	SK-N-SH_RA	brain:	n/a	chr20:52679464-52679485 chr20:52679469-52679487 chr20:52679470-52679486

No data

(count:92 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr20:52239693..52240526-chr20:52678812..52679495,2	MCF-7	breast:
2	chr20:52554098..52560340-chr20:52684210..52688448,9	MCF-7	breast:
3	chr20:52535496..52537138-chr20:52680677..52682336,2	MCF-7	breast:
4	chr17:59476912..59478517-chr20:52679687..52681644,2	MCF-7	breast:
5	chr20:52573995..52574515-chr20:52679072..52679932,2	MCF-7	breast:
6	chr20:52559971..52560523-chr20:52680273..52681108,2	MCF-7	breast:
7	chr20:52679000..52679535-chr20:52692581..52693450,3	MCF-7	breast:
8	chr20:41006906..41008606-chr20:52682135..52684098,2	MCF-7	breast:
9	chr2:26567636..26570065-chr20:52682844..52684382,2	MCF-7	breast:
10	chr20:52683952..52684959-chr20:52701399..52702153,3	MCF-7	breast:
11	chr20:52682759..52688435-chr20:55837866..55842743,7	MCF-7	breast:
12	chr20:52679231..52682277-chr20:52687139..52688972,3	K562	blood:
13	chr20:52683401..52684222-chr22:24971628..24972158,2	MCF-7	breast:
14	chr20:52559378..52561018-chr20:52678965..52680200,31	MCF-7	breast:
15	chr20:52553947..52555886-chr20:52679638..52682394,3	MCF-7	breast:
16	chr20:52680642..52682938-chr20:55848441..55851071,2	MCF-7	breast:
17	chr20:52659902..52660887-chr20:52678920..52680381,7	MCF-7	breast:
18	chr20:52678237..52680834-chr20:52687085..52688960,2	K562	blood:
19	chr11:20042762..20044450-chr20:52683643..52686513,2	MCF-7	breast:
20	chr17:56706894..56712075-chr20:52682647..52687928,11	MCF-7	breast:
21	chr20:52190970..52191876-chr20:52678761..52679613,2	MCF-7	breast:
22	chr20:49404461..49405308-chr20:52679057..52679572,2	MCF-7	breast:
23	chr20:52679100..52679888-chr20:52713261..52713868,2	MCF-7	breast:
24	chr20:52205396..52212193-chr20:52682424..52689159,12	MCF-7	breast:
25	chr20:52679335..52679944-chr20:52712951..52713861,3	MCF-7	breast:
26	chr20:45986431..45988883-chr20:52677453..52680110,2	MCF-7	breast:
27	chr20:52531928..52532988-chr20:52679010..52679629,4	MCF-7	breast:
28	chr20:52683823..52684540-chr20:52815286..52816270,2	MCF-7	breast:
29	chr20:52677507..52680494-chr3:64381929..64383896,2	MCF-7	breast:
30	chr20:52604122..52604816-chr20:52679203..52679933,2	MCF-7	breast:
31	chr20:52676834..52679503-chr20:53266669..53268779,2	MCF-7	breast:
32	chr20:51970413..51971367-chr20:52684017..52684578,2	MCF-7	breast:
33	chr20:46413659..46415494-chr20:52680026..52681756,2	MCF-7	breast:
34	chr20:52212827..52216446-chr20:52677595..52681391,3	MCF-7	breast:
35	chr17:57914792..57916494-chr20:52684237..52686091,2	MCF-7	breast:
36	chr20:52556238..52557068-chr20:52678971..52679960,5	MCF-7	breast:
37	chr20:52561105..52561751-chr20:52678984..52679783,3	MCF-7	breast:
38	chr20:52195073..52195979-chr20:52678957..52680236,7	MCF-7	breast:
39	chr20:52261605..52264321-chr20:52679495..52681960,2	MCF-7	breast:
40	chr17:56707565..56710367-chr20:52679434..52682124,8	MCF-7	breast:
41	chr17:59713185..59713904-chr20:52679512..52680387,2	MCF-7	breast:
42	chr17:56707956..56710519-chr20:52679502..52682472,2	MCF-7	breast:
43	chr20:52195174..52196195-chr20:52679020..52679926,4	MCF-7	breast:
44	chr20:52678982..52679558-chr20:52709556..52710359,2	MCF-7	breast:
45	chr20:46412316..46414537-chr20:52680963..52682540,2	MCF-7	breast:
46	chr20:52679054..52679922-chr20:52815868..52816606,3	MCF-7	breast:
47	chr20:52559216..52560998-chr20:52678738..52679912,14	MCF-7	breast:
48	chr20:52678959..52679775-chr20:52815946..52816831,2	MCF-7	breast:
49	chr20:52684180..52684700-chr20:52739750..52740710,2	MCF-7	breast:
50	chr17:56734557..56739323-chr20:52682038..52691817,18	MCF-7	breast:

No data

miRNA name	Chromosome Location	mirBase accession
hsa-miR-4756-5p	chr20:52684991-52685013	MIMAT0019899
hsa-miR-4756-3p	chr20:52684957-52684978	MIMAT0019900

No data

Variant related genes	Relation type
MIR4756	TF binding region
ENSG00000266826	chromatin interactions
ENSG00000200997	chromatin interactions
ENSG00000064787	chromatin interactions
ENSG00000226308	chromatin interactions
ENSG00000236352	chromatin interactions
ENSG00000267280	chromatin interactions
ENSG00000187013	chromatin interactions
ENSG00000166833	chromatin interactions
ENSG00000121068	chromatin interactions
ENSG00000091831	chromatin interactions
ENSG00000171940	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000267131	chromatin interactions
ENSG00000138018	chromatin interactions
ENSG00000101144	chromatin interactions
ENSG00000196562	chromatin interactions
ENSG00000202077	chromatin interactions
ENSG00000265595	chromatin interactions
ENSG00000173567	chromatin interactions
ENSG00000062716	chromatin interactions

Extended variants
information (count: 328 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:328 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12624748	chr20:52679137-52679138	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs12624750	chr20:52679155-52679156	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs558471143	chr20:52679168-52679169	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs462703	chr20:52679179-52679180	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs77725906	chr20:52679190-52679191	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs560969541	chr20:52679198-52679199	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs146037416	chr20:52679201-52679202	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs539810735	chr20:52679223-52679224	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs138925370	chr20:52679245-52679246	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs532073024	chr20:52679257-52679258	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs555003910	chr20:52679283-52679284	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs458674	chr20:52679327-52679328	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs3787540	chr20:52679330-52679331	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs548622821	chr20:52679368-52679369	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs142923164	chr20:52679370-52679371	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs376015384	chr20:52679395-52679396	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs150380265	chr20:52679422-52679423	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs145616857	chr20:52679459-52679460	Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs290436	chr20:52679492-52679493	Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs571005533	chr20:52679504-52679505	Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs372098115	chr20:52679513-52679514	Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs539931477	chr20:52679577-52679578	Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs534403412	chr20:52679581-52679582	Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs558753217	chr20:52679631-52679632	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs575326103	chr20:52679671-52679672	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs538019488	chr20:52679693-52679694	Weak transcription Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
27	rs377004928	chr20:52679714-52679715	Weak transcription Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
28	rs137874648	chr20:52679719-52679720	Weak transcription Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
29	rs554775392	chr20:52679732-52679733	Weak transcription Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
30	rs6127076	chr20:52679761-52679762	Weak transcription Enhancers	Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs368659193	chr20:52679777-52679778	Weak transcription Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
32	rs537207684	chr20:52679785-52679786	Weak transcription Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
33	rs539886614	chr20:52679788-52679789	Weak transcription Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
34	rs373167616	chr20:52679845-52679846	Weak transcription Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
35	rs557296161	chr20:52679867-52679868	Weak transcription Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
36	rs184714073	chr20:52679906-52679907	Weak transcription Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
37	rs188071770	chr20:52679919-52679920	Weak transcription Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
38	rs462041	chr20:52679920-52679921	Weak transcription Enhancers	Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs111347981	chr20:52679931-52679932	Weak transcription Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
40	rs467321	chr20:52679946-52679947	Weak transcription Enhancers	Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs460317	chr20:52679949-52679950	Weak transcription Enhancers	Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs548723375	chr20:52679951-52679952	Weak transcription Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
43	rs556412020	chr20:52679993-52679994	Weak transcription Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
44	rs562371794	chr20:52680014-52680015	Weak transcription Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
45	rs386815188	chr20:52680020-52680021	Weak transcription Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
46	rs462083	chr20:52680021-52680022	Weak transcription Enhancers	Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs461027	chr20:52680064-52680065	Weak transcription Enhancers	Chromatin interactive region	10 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs539952277	chr20:52680068-52680069	Weak transcription Enhancers	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
49	rs373190420	chr20:52680111-52680112	Weak transcription Enhancers	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
50	rs6127078	chr20:52680118-52680119	Weak transcription Enhancers	Chromatin interactive region	10 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Gastric cancer	17908304	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Urothelial carcinoma	21177765	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	21645411	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	21693616	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Endometrial cancer	22040021	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
colon cancer	17210682	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	22028636	CNVD
Breast cancer	21264507	CNVD
Thyroid cancer	19087340	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Colorectal cancer	19359472	CNVD
Gastric cancer	17167181	CNVD
Myeloproliferative neoplasm	19047681	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Breast cancer	17603634	CNVD
Melanoma	18172304	CNVD
Breast cancer	16608533	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17133270	CNVD
Oral cancer	21386901	CNVD
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	18628472	CNVD
Glioblastoma multiforme	18628472	CNVD
Leukemia	18628472	CNVD
Acute myeloid leukemia	20729466	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Myelodysplastic syndrome	21251322	CNVD
Ductal carcinoma	22052326	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Gastric cancer	20585902	CNVD
Ductal carcinoma	18381933	CNVD
Cancer	21129771	CNVD
Cancer	21183584	CNVD
Non-small cell lung cancer	20864512	CNVD
Ovarian cancer	22174824	CNVD
Lung cancer	16740712	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	16620391	CNVD
Okamoto syndrome	17623483	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Bladder cancer	21909424	CNVD
Biliary cancer	19435499	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Cervical cancer	16585170	CNVD
Ovarian cancer	20844748	CNVD
Hirschsprung''s Disease	21712996	CNVD
Breast cancer	21364760	CNVD
Breast cancer	20459607	CNVD
Gastric cancer	18160780	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:212 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:52645200-52682200	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr20:52669400-52681800	Weak transcription	Gastric	stomach
3	chr20:52674400-52681200	Weak transcription	Rectal Mucosa Donor 29	rectum
4	chr20:52674400-52682000	Weak transcription	Colonic Mucosa	Colon
5	chr20:52675000-52683000	Weak transcription	HepG2	liver
6	chr20:52675400-52679200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr20:52675600-52679200	Weak transcription	K562	blood
8	chr20:52675600-52679600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
9	chr20:52675800-52679600	Weak transcription	Primary B cells from peripheral blood	blood
10	chr20:52676800-52679200	Weak transcription	GM12878-XiMat	blood
11	chr20:52677200-52680000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr20:52677400-52680200	Enhancers	Stomach Mucosa	stomach
13	chr20:52677600-52679400	Enhancers	HSMM	muscle
14	chr20:52677600-52679400	Enhancers	NH-A	brain
15	chr20:52677600-52679400	Enhancers	Osteobl	bone
16	chr20:52677600-52679800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr20:52677600-52679800	Enhancers	HSMMtube	muscle
18	chr20:52677600-52679800	Enhancers	NHDF-Ad	bronchial
19	chr20:52677800-52679400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr20:52677800-52679800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr20:52677800-52679800	Enhancers	Brain Cingulate Gyrus	brain
22	chr20:52677800-52679800	Enhancers	Brain Substantia Nigra	brain
23	chr20:52677800-52680000	Enhancers	Adipose Nuclei	Adipose
24	chr20:52678000-52679800	Enhancers	Fetal Heart	heart
25	chr20:52678200-52679200	Weak transcription	Brain Anterior Caudate	brain
26	chr20:52678200-52680200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr20:52678200-52683800	Weak transcription	HMEC	breast
28	chr20:52678200-52684400	Weak transcription	Fetal Stomach	stomach
29	chr20:52678400-52683200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr20:52678800-52680000	Enhancers	Rectal Mucosa Donor 31	rectum
31	chr20:52679000-52679800	Enhancers	Brain Angular Gyrus	brain
32	chr20:52679000-52679800	Enhancers	Brain Hippocampus Middle	brain
33	chr20:52679000-52679800	Enhancers	Brain Inferior Temporal Lobe	brain
34	chr20:52679000-52680000	Enhancers	A549	lung
35	chr20:52679200-52679400	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr20:52679200-52679600	Enhancers	Brain Anterior Caudate	brain
37	chr20:52679200-52679800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr20:52679200-52679800	Enhancers	K562	blood
39	chr20:52679200-52680200	Enhancers	GM12878-XiMat	blood
40	chr20:52679200-52680800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr20:52679200-52681600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
42	chr20:52679400-52683000	Weak transcription	HSMM	muscle
43	chr20:52679400-52683000	Weak transcription	NH-A	brain
44	chr20:52679600-52680800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
45	chr20:52679600-52680800	Enhancers	Primary T cells fromperipheralblood	blood
46	chr20:52679600-52681400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
47	chr20:52679600-52682200	Enhancers	Primary B cells from peripheral blood	blood
48	chr20:52679600-52682200	Enhancers	Primary hematopoietic stem cells	blood
49	chr20:52679600-52682400	Enhancers	Primary hematopoietic stem cells short term culture	blood
50	chr20:52679600-52682600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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