Variant report

Variant	nsv825771
Chromosome Location	chr11:17027229-17048360
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:602)
CpG islands
(count:854)
Chromatin interactive
region (count:22)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:602 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:17036440-17037210	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:17036145-17036156	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:17040701-17040761	HepG2	liver:	n/a	n/a
4	ARID3A	chr11:17034308-17034849	HepG2	liver:	n/a	n/a
5	ATF1	chr11:17041401-17041436	K562	blood:	n/a	n/a
6	ATF3	chr11:17034359-17034857	A549	lung:	n/a	n/a
7	BACH1	chr11:17034566-17035293	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr11:17035550-17035605	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr11:17036133-17036192	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCL3	chr11:17036715-17037219	A549	lung:	n/a	n/a
11	BCL3	chr11:17034242-17034926	A549	lung:	n/a	n/a
12	BCL3	chr11:17034009-17034854	A549	lung:	n/a	n/a
13	BCL3	chr11:17036311-17036869	A549	lung:	n/a	chr11:17036590-17036599
14	BHLHE40	chr11:17036486-17037136	HepG2	liver:	n/a	n/a
15	BHLHE40	chr11:17043073-17043359	K562	blood:	n/a	n/a
16	CEBPB	chr11:17034245-17034871	A549	lung:	n/a	chr11:17034449-17034460
17	CEBPB	chr11:17034071-17034889	MCF-7	breast:	n/a	chr11:17034449-17034460
18	CEBPB	chr11:17029631-17029945	IMR90	lung:	n/a	chr11:17029775-17029786
19	CEBPB	chr11:17045547-17045751	HepG2	liver:	n/a	chr11:17045655-17045666 chr11:17045654-17045665
20	CEBPB	chr11:17034231-17034780	HepG2	liver:	n/a	chr11:17034449-17034460
21	CEBPB	chr11:17042906-17043146	K562	blood:	n/a	n/a
22	CEBPB	chr11:17034246-17034919	MCF-7	breast:	n/a	chr11:17034449-17034460
23	CEBPB	chr11:17042879-17043169	HepG2	liver:	n/a	n/a
24	CEBPB	chr11:17029625-17029959	HepG2	liver:	n/a	chr11:17029775-17029786
25	CEBPB	chr11:17042869-17043314	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr11:17034064-17035027	A549	lung:	n/a	chr11:17034449-17034460
27	CEBPB	chr11:17034449-17034468	K562	blood:	n/a	chr11:17034449-17034460
28	CEBPB	chr11:17034274-17034688	IMR90	lung:	n/a	chr11:17034449-17034460
29	CEBPB	chr11:17029607-17029938	Hela-S3	cervix:	n/a	chr11:17029775-17029786
30	CEBPB	chr11:17029603-17029969	MCF-7	breast:	n/a	chr11:17029775-17029786
31	CEBPB	chr11:17042956-17043438	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr11:17033606-17033706	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr11:17029632-17029948	A549	lung:	n/a	chr11:17029775-17029786
34	CEBPB	chr11:17034340-17034519	Hela-S3	cervix:	n/a	chr11:17034449-17034460
35	CEBPB	chr11:17034193-17034816	A549	lung:	n/a	chr11:17034449-17034460
36	CEBPB	chr11:17029688-17029854	H1-hESC	embryonic stem cell:	n/a	chr11:17029775-17029786
37	CEBPD	chr11:17034466-17034824	HepG2	liver:	n/a	n/a
38	CEBPD	chr11:17036007-17036401	HepG2	liver:	n/a	n/a
39	CEBPD	chr11:17034926-17035668	HepG2	liver:	n/a	n/a
40	CHD1	chr11:17035596-17035599	H1-hESC	embryonic stem cell:	n/a	n/a
41	CHD2	chr11:17035272-17035452	HepG2	liver:	n/a	chr11:17035441-17035451
42	CHD2	chr11:17036526-17036750	HepG2	liver:	n/a	n/a
43	CHD2	chr11:17034552-17035054	HepG2	liver:	n/a	n/a
44	CHD2	chr11:17036167-17036308	HepG2	liver:	n/a	n/a
45	CREB1	chr11:17034354-17035789	A549	lung:	n/a	n/a
46	CREB1	chr11:17034380-17034735	A549	lung:	n/a	n/a
47	CREB1	chr11:17035875-17036268	A549	lung:	n/a	n/a
48	CREB1	chr11:17036550-17036832	A549	lung:	n/a	n/a
49	CTBP2	chr11:17034437-17035493	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr11:17036700-17036850	HCPEpiC	choroid plexus:	n/a	chr11:17036768-17036786

(count:854 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:17036042-17036092	HCM	heart:	n/a
2	chr11:17035411-17035461	SK-N-SH_RA	brain:	n/a
3	chr11:17032483-17032533	AG04449	skin:	fetal
4	chr11:17034644-17034694	NT2-D1	testis:	n/a
5	chr11:17034644-17034694	Caco-2	colon:	n/a
6	chr11:17036644-17036694	AG04449	skin:	fetal
7	chr11:17036403-17036453	GM12891	blood:	n/a
8	chr11:17036042-17036092	A549	lung:	n/a
9	chr11:17036581-17036631	HRPEpiC	eye:	n/a
10	chr11:17036644-17036694	RPTEC	kidney:	n/a
11	chr11:17032483-17032533	GM12878	blood:	n/a
12	chr11:17036042-17036092	AG09309	skin:	n/a
13	chr11:17035779-17035829	NH-A	brain:	n/a
14	chr11:17035779-17035829	A549	lung:	n/a
15	chr11:17036337-17036387	ovcar-3	ovarian:	n/a
16	chr11:17036137-17036187	U87	brain:	n/a
17	chr11:17035876-17035926	SK-N-SH	brain:	n/a
18	chr11:17036042-17036092	HRCEpiC	kidney:	n/a
19	chr11:17036137-17036187	HEK293	kidney:	embryo
20	chr11:17036644-17036694	HUVEC	blood vessel:	n/a
21	chr11:17034844-17034894	ECC-1	luminal epithelium:	n/a
22	chr11:17036403-17036453	AG04450	lung:	fetal
23	chr11:17036403-17036453	HCM	heart:	n/a
24	chr11:17036644-17036694	HRCEpiC	kidney:	n/a
25	chr11:17036644-17036694	IMR90	lung:	fetal
26	chr11:17035876-17035926	Hela-S3	cervix:	n/a
27	chr11:17036403-17036453	K562	blood:	n/a
28	chr11:17035411-17035461	AG10803	skin:	n/a
29	chr11:17036142-17036192	BJ	skin:	n/a
30	chr11:17034484-17034534	HepG2	liver:	n/a
31	chr11:17035876-17035926	HRE	kidney:	n/a
32	chr11:17035876-17035926	H1-hESC	embryonic stem cell:	embryo
33	chr11:17034484-17034534	GM06990	blood:	n/a
34	chr11:17034644-17034694	PANC-1	pancreas:	n/a
35	chr11:17035779-17035829	BJ	skin:	n/a
36	chr11:17035779-17035829	HCM	heart:	n/a
37	chr11:17036337-17036387	GM12878	blood:	n/a
38	chr11:17034644-17034694	NH-A	brain:	n/a
39	chr11:17034484-17034534	U87	brain:	n/a
40	chr11:17036644-17036694	NT2-D1	testis:	n/a
41	chr11:17036403-17036453	Jurkat	blood:	n/a
42	chr11:17036337-17036387	PANC-1	pancreas:	n/a
43	chr11:17036137-17036187	HCT-116	colon:	n/a
44	chr11:17036581-17036631	NH-A	brain:	n/a
45	chr11:17034644-17034694	NHBE	bronchial:	n/a
46	chr11:17036142-17036192	MCF10A-Er-Src	breast:	n/a
47	chr11:17036644-17036694	NHDF-neo	bronchial:	n/a
48	chr11:17036142-17036192	NHBE	bronchial:	n/a
49	chr11:17036142-17036192	HCM	heart:	n/a
50	chr11:17035411-17035461	Hepatocyte	liver:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:17025213..17027941-chr11:17028689..17031189,2	K562	blood:
2	chr11:17043020..17045707-chr11:17047002..17049137,2	MCF-7	breast:
3	chr11:17037168..17039319-chr11:17083342..17085313,2	MCF-7	breast:
4	chr11:17025721..17027446-chr11:17098027..17100725,2	MCF-7	breast:
5	chr11:17027622..17030583-chr11:17098379..17100590,2	K562	blood:
6	chr11:17018572..17027460-chr11:17032241..17037685,12	MCF-7	breast:
7	chr11:16995340..16999228-chr11:17033547..17036418,3	MCF-7	breast:
8	chr11:17043020..17045707-chr11:17047002..17049137,2	MCF-7	breast:
9	chr11:17031613..17034437-chr11:17043596..17045738,2	MCF-7	breast:
10	chr11:17012348..17014489-chr11:17025477..17027730,2	MCF-7	breast:
11	chr11:17040265..17042474-chr11:17045522..17047105,2	K562	blood:
12	chr11:17040265..17042474-chr11:17045522..17047105,2	K562	blood:
13	chr11:17031613..17034437-chr11:17043596..17045738,2	MCF-7	breast:
14	chr11:17000031..17001967-chr11:17030020..17032761,3	MCF-7	breast:
15	chr11:17042951..17044866-chr11:17096033..17099026,2	MCF-7	breast:
16	chr11:16988453..16990354-chr11:17039773..17042138,2	MCF-7	breast:
17	chr11:17008749..17010885-chr11:17026366..17028840,2	MCF-7	breast:
18	chr11:16967271..16967926-chr11:17036420..17037064,2	MCF-7	breast:
19	chr11:16994632..16996478-chr11:17034698..17036230,2	MCF-7	breast:
20	chr11:17034691..17036893-chr11:17040088..17042253,2	K562	blood:
21	chr11:17034631..17037564-chr11:17097951..17099758,2	MCF-7	breast:
22	chr11:16978078..16978699-chr11:17032228..17032731,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NUCB2-6	chr11:17042246-17043656	NONHSAT018198
2	lnc-NUCB2-7	chr11:17035545-17035914	NONHSAT018197

No data

Variant related genes	Relation type
PLEKHA7	TF binding region
ENSG00000266493	TF binding region
OR7E14P	TF binding region
PLEKHA7	CpG island
ENSG00000266493	CpG island
OR7E14P	CpG island
ENSG00000272034	chromatin interactions
ENSG00000244398	chromatin interactions
ENSG00000166689	chromatin interactions
ENSG00000266493	chromatin interactions
ENSG00000184669	chromatin interactions
ENSG00000251928	chromatin interactions
ENSG00000201403	chromatin interactions
ENSG00000110700	chromatin interactions

Extended variants
information (count: 831 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:831 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs371464538	chr11:17027262-17027263	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs530655094	chr11:17027265-17027266	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs548788075	chr11:17027287-17027288	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs34819854	chr11:17027298-17027299	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs534806070	chr11:17027300-17027301	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs10741719	chr11:17027329-17027330	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs183090914	chr11:17027331-17027332	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs538523753	chr11:17027335-17027336	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs10741720	chr11:17027429-17027430	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs573529866	chr11:17027430-17027431	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs148700751	chr11:17027465-17027466	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs373612886	chr11:17027510-17027511	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs555433929	chr11:17027533-17027534	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs10734250	chr11:17027555-17027556	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs187427660	chr11:17027573-17027574	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs35053700	chr11:17027639-17027640	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs10741721	chr11:17027653-17027654	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs533465413	chr11:17027666-17027667	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs4757485	chr11:17027688-17027689	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs563330728	chr11:17027714-17027715	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs563091290	chr11:17027715-17027716	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs35246294	chr11:17027742-17027743	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs530414456	chr11:17027744-17027745	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs190380405	chr11:17027746-17027747	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs560967071	chr11:17027750-17027751	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs542375315	chr11:17027763-17027764	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs111689608	chr11:17027773-17027774	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs559862260	chr11:17027779-17027780	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs546833747	chr11:17027780-17027781	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs113506663	chr11:17027796-17027797	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs4757486	chr11:17027805-17027806	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs182798762	chr11:17027824-17027825	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs563917593	chr11:17027849-17027850	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs570076427	chr11:17027888-17027889	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs528350333	chr11:17027894-17027895	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs143371469	chr11:17027901-17027902	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs573810026	chr11:17027942-17027943	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs546891546	chr11:17027948-17027949	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs553176210	chr11:17027983-17027984	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs10832715	chr11:17028003-17028004	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs35511252	chr11:17028020-17028021	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs545724272	chr11:17028030-17028031	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs71484746	chr11:17028037-17028038	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs575847141	chr11:17028038-17028039	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs542655339	chr11:17028043-17028044	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs10832716	chr11:17028070-17028071	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs528217894	chr11:17028079-17028080	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs546697372	chr11:17028098-17028099	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs565113273	chr11:17028100-17028101	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs532200558	chr11:17028136-17028137	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:53)

Disease	PMID	Source
Cancer	21183584	CNVD
Gastric adenocarcinoma	19115996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Multiple myeloma	16461302	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21858162	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
Lung adenocarcinoma	17086460	CNVD
Urothelial cell carcinoma	18451213	CNVD
Lung cancer	17086460	CNVD
Uterine serous papillary cancer	19536090	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:799 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:17004800-17034200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr11:17006400-17034000	Weak transcription	Brain Cingulate Gyrus	brain
3	chr11:17009400-17032600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr11:17009800-17030000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr11:17009800-17032600	Weak transcription	HUES48 Cell Line	embryonic stem cell
6	chr11:17009800-17032600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr11:17013400-17033800	Weak transcription	Brain Substantia Nigra	brain
8	chr11:17016400-17034600	Weak transcription	Aorta	Aorta
9	chr11:17016600-17030800	Weak transcription	Fetal Kidney	kidney
10	chr11:17018000-17028000	Weak transcription	Stomach Smooth Muscle	stomach
11	chr11:17018000-17029400	Weak transcription	Brain Anterior Caudate	brain
12	chr11:17018800-17032000	Weak transcription	Fetal Muscle Leg	muscle
13	chr11:17019000-17032600	Weak transcription	H1 Cell Line	embryonic stem cell
14	chr11:17019400-17034800	Weak transcription	Lung	lung
15	chr11:17019800-17034600	Weak transcription	Right Ventricle	heart
16	chr11:17021000-17034000	Weak transcription	Rectal Mucosa Donor 29	rectum
17	chr11:17021000-17034200	Weak transcription	Colonic Mucosa	Colon
18	chr11:17021200-17034600	Weak transcription	Right Atrium	heart
19	chr11:17021400-17030400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr11:17022000-17034600	Weak transcription	Brain Angular Gyrus	brain
21	chr11:17023200-17028600	Weak transcription	Left Ventricle	heart
22	chr11:17023200-17032600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr11:17023200-17033600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr11:17023800-17028400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr11:17024000-17029600	Weak transcription	Fetal Stomach	stomach
26	chr11:17025200-17027400	Enhancers	Stomach Mucosa	stomach
27	chr11:17025200-17027800	Enhancers	HepG2	liver
28	chr11:17025600-17029600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr11:17025600-17029800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr11:17025600-17032600	Weak transcription	Duodenum Mucosa	Duodenum
31	chr11:17026000-17029600	Weak transcription	Fetal Intestine Large	intestine
32	chr11:17026600-17027800	Enhancers	Breast Myoepithelial Primary Cells	Breast
33	chr11:17026800-17027600	Weak transcription	Pancreas	Pancrea
34	chr11:17026800-17028400	Strong transcription	A549	lung
35	chr11:17026800-17029600	Weak transcription	Gastric	stomach
36	chr11:17026800-17032200	Strong transcription	Fetal Intestine Small	intestine
37	chr11:17027000-17027800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr11:17027000-17029200	Weak transcription	Liver	Liver
39	chr11:17027200-17027400	Enhancers	Adipose Nuclei	Adipose
40	chr11:17027200-17027600	Enhancers	Small Intestine	intestine
41	chr11:17027200-17028400	Weak transcription	Sigmoid Colon	Sigmoid Colon
42	chr11:17027200-17029600	Weak transcription	Rectal Mucosa Donor 31	rectum
43	chr11:17027200-17029800	Weak transcription	Esophagus	oesophagus
44	chr11:17027400-17029600	Weak transcription	Adipose Nuclei	Adipose
45	chr11:17027400-17029600	Weak transcription	Stomach Mucosa	stomach
46	chr11:17027600-17028800	Enhancers	Pancreas	Pancrea
47	chr11:17027800-17029200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
48	chr11:17027800-17029800	Weak transcription	HepG2	liver
49	chr11:17027800-17032800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr11:17028400-17028600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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