Variant report

Variant	nsv1036541
Chromosome Location	chr11:48091589-48116032
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:319)
CpG islands
(count:122)
Chromatin interactive
region (count:28)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:319 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:48114969-48116284	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:48095041-48095124	K562	blood:	n/a	n/a
3	ATF2	chr11:48094862-48095450	GM12878	blood:	n/a	n/a
4	BACH1	chr11:48110331-48110562	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr11:48115348-48115634	GM12878	blood:	n/a	n/a
6	BATF	chr11:48094903-48095273	GM12878	blood:	n/a	n/a
7	BCL11A	chr11:48115355-48115560	GM12878	blood:	n/a	n/a
8	BCL3	chr11:48115343-48115664	GM12878	blood:	n/a	n/a
9	BCLAF1	chr11:48094857-48095248	GM12878	blood:	n/a	n/a
10	BCLAF1	chr11:48115236-48115686	GM12878	blood:	n/a	n/a
11	BHLHE40	chr11:48115378-48115650	K562	blood:	n/a	n/a
12	BHLHE40	chr11:48103167-48103191	K562	blood:	n/a	n/a
13	BRCA1	chr11:48093751-48093761	HepG2	liver:	n/a	n/a
14	CEBPB	chr11:48096132-48096309	K562	blood:	n/a	chr11:48096193-48096206
15	CEBPB	chr11:48096050-48096341	Hela-S3	cervix:	n/a	chr11:48096193-48096206
16	CEBPB	chr11:48115956-48116106	HepG2	liver:	n/a	n/a
17	CEBPB	chr11:48104258-48104526	HepG2	liver:	n/a	chr11:48104338-48104349 chr11:48104335-48104352
18	CHD2	chr11:48094837-48094838	GM12878	blood:	n/a	n/a
19	CTCF	chr11:48102800-48102950	AG04449	skin:	n/a	n/a
20	CTCF	chr11:48102720-48102870	AG09309	skin:	n/a	chr11:48102792-48102805
21	CTCF	chr11:48102720-48102870	RPTEC	kidney:	n/a	chr11:48102792-48102805
22	CTCF	chr11:48102680-48102830	HCFaa	heart:	n/a	chr11:48102792-48102805
23	CTCF	chr11:48102760-48102910	AG09319	gingival:	n/a	chr11:48102792-48102805
24	CTCF	chr11:48102660-48102810	HAc	cerebellar:	n/a	chr11:48102792-48102805
25	CTCF	chr11:48113000-48113150	GM12866	blood:	n/a	n/a
26	CTCF	chr11:48101380-48101530	GM12865	blood:	n/a	n/a
27	CTCF	chr11:48102600-48102750	RPTEC	kidney:	n/a	n/a
28	CTCF	chr11:48102820-48102847	ProgFib	skin:	n/a	n/a
29	CTCF	chr11:48102540-48102690	GM12864	blood:	n/a	n/a
30	CTCF	chr11:48102700-48102850	HRE	kidney:	n/a	chr11:48102792-48102805
31	CTCF	chr11:48102660-48102810	AG09309	skin:	n/a	chr11:48102792-48102805
32	CTCF	chr11:48102680-48102830	HPAF	blood vessel:	n/a	chr11:48102792-48102805
33	CTCF	chr11:48102780-48102930	HBMEC	blood vessel:	n/a	chr11:48102792-48102805
34	CTCF	chr11:48102720-48102870	HCPEpiC	choroid plexus:	n/a	chr11:48102792-48102805
35	CTCF	chr11:48102760-48102910	AG10803	skin:	n/a	chr11:48102792-48102805
36	CTCF	chr11:48102720-48102870	HRPEpiC	eye:	n/a	chr11:48102792-48102805
37	CTCF	chr11:48102780-48102886	Fibrobl	skin:	n/a	chr11:48102792-48102805
38	CTCF	chr11:48102780-48102930	AoAF	blood vessel:	n/a	chr11:48102792-48102805
39	CTCF	chr11:48102660-48102810	AG10803	skin:	n/a	chr11:48102792-48102805
40	CTCF	chr11:48102800-48102950	HRE	kidney:	n/a	n/a
41	CUX1	chr11:48096147-48096247	K562	blood:	n/a	n/a
42	CUX1	chr11:48115384-48115504	K562	blood:	n/a	n/a
43	CUX1	chr11:48115366-48115523	GM12878	blood:	n/a	n/a
44	CUX1	chr11:48095078-48095249	GM12878	blood:	n/a	n/a
45	E2F4	chr11:48108442-48108590	MCF10A-Er-Src	breast:	n/a	n/a
46	EBF1	chr11:48102565-48102873	GM12878	blood:	n/a	n/a
47	EBF1	chr11:48115926-48116051	GM12878	blood:	n/a	n/a
48	ELF1	chr11:48102554-48102912	GM12878	blood:	n/a	n/a
49	EP300	chr11:48114714-48114743	GM12878	blood:	n/a	n/a
50	EP300	chr11:48102444-48103230	SK-N-SH	brain:	n/a	chr11:48102966-48102976 chr11:48102926-48102940

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:48110045-48110095	GM19239	blood:	n/a
2	chr11:48110045-48110095	SK-N-MC	brain:	n/a
3	chr11:48110045-48110095	HCF	heart:	n/a
4	chr11:48112253-48112303	MCF-7	breast:	n/a
5	chr11:48110045-48110095	BE2_C	brain:	n/a
6	chr11:48112253-48112303	ovcar-3	ovarian:	n/a
7	chr11:48112253-48112303	NHBE	bronchial:	n/a
8	chr11:48110045-48110095	HRPEpiC	eye:	n/a
9	chr11:48112253-48112303	NB4	blood:	n/a
10	chr11:48112253-48112303	HPAEpiC	pulmonary alveolar:	n/a
11	chr11:48112253-48112303	SK-N-MC	brain:	n/a
12	chr11:48112253-48112303	HCF	heart:	n/a
13	chr11:48110045-48110095	HMEC	breast:	n/a
14	chr11:48110045-48110095	GM12878	blood:	n/a
15	chr11:48110045-48110095	HUVEC	blood vessel:	n/a
16	chr11:48110045-48110095	PANC-1	pancreas:	n/a
17	chr11:48110045-48110095	HRE	kidney:	n/a
18	chr11:48112253-48112303	SAEC	small airway:	n/a
19	chr11:48112253-48112303	CMK	blood:	n/a
20	chr11:48110045-48110095	NHBE	bronchial:	n/a
21	chr11:48110045-48110095	HRCEpiC	kidney:	n/a
22	chr11:48110045-48110095	HCPEpiC	choroid plexus:	n/a
23	chr11:48110045-48110095	T-47D	breast:	n/a
24	chr11:48112253-48112303	PFSK-1	brain:	n/a
25	chr11:48110045-48110095	HIPEpiC	eye:	n/a
26	chr11:48110045-48110095	Caco-2	colon:	n/a
27	chr11:48110045-48110095	RPTEC	kidney:	n/a
28	chr11:48110045-48110095	ProgFib	skin:	n/a
29	chr11:48110045-48110095	MCF-7	breast:	n/a
30	chr11:48112253-48112303	K562	blood:	n/a
31	chr11:48112253-48112303	GM12878	blood:	n/a
32	chr11:48112253-48112303	HMEC	breast:	n/a
33	chr11:48110045-48110095	ovcar-3	ovarian:	n/a
34	chr11:48112253-48112303	SK-N-SH	brain:	n/a
35	chr11:48112253-48112303	Caco-2	colon:	n/a
36	chr11:48112253-48112303	AG10803	skin:	n/a
37	chr11:48110045-48110095	HPAEpiC	pulmonary alveolar:	n/a
38	chr11:48110045-48110095	HEEpiC	esophagus:	n/a
39	chr11:48112253-48112303	GM19239	blood:	n/a
40	chr11:48112253-48112303	AoSMC	blood vessel:	n/a
41	chr11:48110045-48110095	MCF10A-Er-Src	breast:	n/a
42	chr11:48110045-48110095	Hela-S3	cervix:	n/a
43	chr11:48112253-48112303	AG09319	gingival:	n/a
44	chr11:48110045-48110095	HCM	heart:	n/a
45	chr11:48110045-48110095	GM06990	blood:	n/a
46	chr11:48112253-48112303	Hela-S3	cervix:	n/a
47	chr11:48112253-48112303	NHDF-neo	bronchial:	n/a
48	chr11:48112253-48112303	HEK293	kidney:	embryo
49	chr11:48112253-48112303	HAEpiC	amniotic membrane:	n/a
50	chr11:48110045-48110095	NH-A	brain:	n/a

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:48105031..48106761-chr11:48108023..48109885,2	MCF-7	breast:
2	chr11:48098800..48100999-chr11:48104120..48106582,2	MCF-7	breast:
3	chr11:48087146..48090054-chr11:48094817..48096585,2	MCF-7	breast:
4	chr11:48097619..48099123-chr11:48100995..48103478,2	MCF-7	breast:
5	chr11:48047876..48049953-chr11:48109269..48111434,2	MCF-7	breast:
6	chr11:48101649..48104254-chr11:48106713..48109745,3	MCF-7	breast:
7	chr11:48081533..48083185-chr11:48091579..48093994,2	MCF-7	breast:
8	chr11:48092743..48095466-chr11:48097566..48099297,2	K562	blood:
9	chr11:48112031..48113821-chr11:48114417..48116008,2	K562	blood:
10	chr11:48093831..48096549-chr11:48096756..48099477,2	MCF-7	breast:
11	chr11:48098800..48100999-chr11:48104120..48106582,2	MCF-7	breast:
12	chr11:48086913..48088924-chr11:48093954..48095544,2	K562	blood:
13	chr11:48101649..48104254-chr11:48106713..48109745,3	MCF-7	breast:
14	chr11:48093831..48096549-chr11:48096756..48099477,2	MCF-7	breast:
15	chr11:48108133..48109846-chr11:48110400..48112858,3	MCF-7	breast:
16	chr11:48001457..48003735-chr11:48105234..48107341,2	K562	blood:
17	chr11:48108133..48109846-chr11:48110400..48112858,3	MCF-7	breast:
18	chr11:48112031..48113821-chr11:48114417..48116008,2	K562	blood:
19	chr11:48092743..48095466-chr11:48097566..48099297,2	K562	blood:
20	chr11:48109181..48111732-chr11:48113222..48115393,2	K562	blood:
21	chr11:48082980..48084917-chr11:48096551..48099093,2	K562	blood:
22	chr11:48107721..48110377-chr11:48121800..48123863,2	MCF-7	breast:
23	chr11:48099180..48102059-chr11:48102708..48105162,2	K562	blood:
24	chr11:48109181..48111732-chr11:48113222..48115393,2	K562	blood:
25	chr11:48105031..48106761-chr11:48108023..48109885,2	MCF-7	breast:
26	chr11:48099180..48102059-chr11:48102708..48105162,2	K562	blood:
27	chr11:48097619..48099123-chr11:48100995..48103478,2	MCF-7	breast:
28	chr11:48083070..48085451-chr11:48088899..48092016,4	K562	blood:

No data

Variant related genes	Relation type
MIR3161	TF binding region
MIR3161	CpG island
ENSG00000149177	chromatin interactions

Extended variants
information (count: 824 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:824 , 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	rs190666643	chr11:48091603-48091604	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs533794536	chr11:48091626-48091627	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs554413515	chr11:48091627-48091628	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs74777509	chr11:48091628-48091629	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs183827674	chr11:48091629-48091630	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs78030441	chr11:48091632-48091633	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs576462870	chr11:48091664-48091665	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs374004328	chr11:48091677-48091678	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs535579720	chr11:48091681-48091682	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs7395231	chr11:48091689-48091690	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs572074030	chr11:48091753-48091754	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs541034689	chr11:48091763-48091764	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs61914736	chr11:48091778-48091779	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs577111942	chr11:48091779-48091780	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs545969228	chr11:48091780-48091781	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs146514166	chr11:48091781-48091782	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs532218601	chr11:48091788-48091789	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs551953651	chr11:48091793-48091794	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs548281777	chr11:48091800-48091801	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs370256258	chr11:48091845-48091846	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs562299789	chr11:48091848-48091849	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs113252984	chr11:48091927-48091928	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs7358469	chr11:48091929-48091930	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs531515688	chr11:48091966-48091967	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs144606134	chr11:48091975-48091976	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs10769310	chr11:48091976-48091977	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs571113783	chr11:48092023-48092024	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs567998635	chr11:48092028-48092029	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs372452513	chr11:48092053-48092054	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs35904394	chr11:48092071-48092072	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs550325114	chr11:48092141-48092142	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs545200849	chr11:48092152-48092153	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs34237177	chr11:48092237-48092238	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs569885330	chr11:48092294-48092295	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs535666578	chr11:48092309-48092310	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs188770691	chr11:48092336-48092337	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs555401029	chr11:48092359-48092360	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs140211253	chr11:48092498-48092499	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs535014477	chr11:48092527-48092528	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs557907089	chr11:48092548-48092549	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs577053095	chr11:48092565-48092566	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs545808596	chr11:48092620-48092621	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs193283865	chr11:48092666-48092667	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs533773344	chr11:48092671-48092672	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs547223498	chr11:48092693-48092694	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs367578352	chr11:48092696-48092697	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs370790714	chr11:48092736-48092737	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs80209692	chr11:48092740-48092741	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs182526068	chr11:48092835-48092836	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs374816473	chr11:48092929-48092930	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Parathyroid adenoma	22454399	CNVD
Medulloblastoma	21979893	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
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Chordoma	18071362	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
small cell lung cancer	20016488	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Myelofibrosis	22110671	CNVD
Melanoma	18172304	CNVD
Intracranial ependymoma	16609018	CNVD
Myxofibrosarcoma	16751306	CNVD
Potocki-Shaffer syndrome	22470819	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	16608533	CNVD
Hirschsprung''s Disease	21712996	CNVD
Follicular lymphoma	20505157	CNVD
Colorectal cancer	21128281	CNVD
Breast cancer	20409316	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17160897	CNVD
Mantle cell lymphoma	19029149	CNVD
Glioblastoma multiforme	21138945	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22581003	CNVD
Glioblastoma multiforme	21390271	CNVD
Acute lymphoblastic leukemia	20699438	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	21990379	CNVD

Chromatin state (count:852 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:48078800-48093000	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr11:48079200-48102800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr11:48080600-48100800	Weak transcription	Spleen	Spleen
4	chr11:48081200-48094600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
5	chr11:48081600-48097200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr11:48081800-48101600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
7	chr11:48082000-48096000	Weak transcription	Pancreatic Islets	Pancreatic Islet
8	chr11:48085800-48094600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
9	chr11:48086000-48094800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
10	chr11:48086000-48100800	Weak transcription	Rectal Mucosa Donor 31	rectum
11	chr11:48086000-48102000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
12	chr11:48086000-48109200	Weak transcription	Fetal Intestine Large	intestine
13	chr11:48086200-48098800	Weak transcription	Primary T cells fromperipheralblood	blood
14	chr11:48086200-48100000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr11:48086200-48101000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr11:48086200-48101000	Weak transcription	Skeletal Muscle Female	skeletal muscle
17	chr11:48086200-48102000	Weak transcription	Duodenum Smooth Muscle	Duodenum
18	chr11:48086200-48114400	Weak transcription	Hela-S3	cervix
19	chr11:48086400-48101000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr11:48086800-48102800	Weak transcription	Rectal Smooth Muscle	rectum
21	chr11:48087000-48100800	Weak transcription	Pancreas	Pancrea
22	chr11:48088400-48098800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr11:48089000-48091800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
24	chr11:48089000-48093600	Weak transcription	Gastric	stomach
25	chr11:48089000-48094600	Weak transcription	Lung	lung
26	chr11:48089000-48102200	Weak transcription	NHDF-Ad	bronchial
27	chr11:48089000-48105800	Weak transcription	Sigmoid Colon	Sigmoid Colon
28	chr11:48089200-48096200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
29	chr11:48089200-48100200	Weak transcription	Fetal Stomach	stomach
30	chr11:48089200-48108000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
31	chr11:48089400-48098800	Weak transcription	Osteobl	bone
32	chr11:48089400-48102400	Weak transcription	HSMM	muscle
33	chr11:48089600-48091600	Strong transcription	Primary B cells from cord blood	blood
34	chr11:48089600-48092800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
35	chr11:48089600-48096200	Weak transcription	Primary T helper cells fromperipheralblood	blood
36	chr11:48089600-48096400	Weak transcription	Brain Anterior Caudate	brain
37	chr11:48089600-48099800	Weak transcription	Brain Angular Gyrus	brain
38	chr11:48089800-48096200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
39	chr11:48089800-48099200	Weak transcription	Brain Hippocampus Middle	brain
40	chr11:48089800-48100000	Weak transcription	Brain Inferior Temporal Lobe	brain
41	chr11:48089800-48100000	Weak transcription	Brain Substantia Nigra	brain
42	chr11:48089800-48100400	Weak transcription	Brain Cingulate Gyrus	brain
43	chr11:48090000-48098800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr11:48090200-48091600	Strong transcription	Primary monocytes fromperipheralblood	blood
45	chr11:48090200-48091800	Strong transcription	Fetal Intestine Small	intestine
46	chr11:48090200-48092200	Strong transcription	Monocytes-CD14+_RO01746	blood
47	chr11:48090200-48092400	Strong transcription	Primary T helper cells PMA-I stimulated	--
48	chr11:48090200-48092400	Strong transcription	Liver	Liver
49	chr11:48090400-48091800	Strong transcription	Primary B cells from peripheral blood	blood
50	chr11:48090400-48094600	Weak transcription	Adipose Nuclei	Adipose

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