Variant report

Variant	nsv896988
Chromosome Location	chr11:9912052-10012511
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1176)
CpG islands
(count:305)
Chromatin interactive
region (count:23)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1176 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:10012155-10012488	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:9972006-9972363	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:9927956-9928592	HepG2	liver:	n/a	n/a
4	ARID3A	chr11:9954531-9954676	HepG2	liver:	n/a	n/a
5	ARID3A	chr11:9952406-9952773	HepG2	liver:	n/a	n/a
6	ATF1	chr11:9921913-9921972	K562	blood:	n/a	n/a
7	ATF1	chr11:9978223-9978390	K562	blood:	n/a	n/a
8	ATF1	chr11:9952454-9952810	K562	blood:	n/a	n/a
9	ATF2	chr11:9984115-9984704	GM12878	blood:	n/a	n/a
10	ATF2	chr11:9944102-9944787	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr11:9984169-9984650	GM12878	blood:	n/a	n/a
12	ATF3	chr11:9927407-9928463	A549	lung:	n/a	n/a
13	ATF3	chr11:10004659-10005096	A549	lung:	n/a	n/a
14	ATF3	chr11:9927327-9928521	A549	lung:	n/a	n/a
15	BACH1	chr11:9944284-9944722	H1-hESC	embryonic stem cell:	n/a	n/a
16	BATF	chr11:9969025-9969393	GM12878	blood:	n/a	n/a
17	BATF	chr11:9984302-9984676	GM12878	blood:	n/a	n/a
18	BATF	chr11:9994519-9994792	GM12878	blood:	n/a	chr11:9994688-9994697
19	BCL11A	chr11:9927609-9927908	H1-hESC	embryonic stem cell:	n/a	n/a
20	BCL3	chr11:9927385-9928510	A549	lung:	n/a	n/a
21	BCL3	chr11:10004548-10005126	A549	lung:	n/a	n/a
22	BCL3	chr11:10004437-10005076	A549	lung:	n/a	n/a
23	BCL3	chr11:9927314-9928646	A549	lung:	n/a	n/a
24	BCLAF1	chr11:9984271-9984598	GM12878	blood:	n/a	n/a
25	BCLAF1	chr11:9984166-9984674	GM12878	blood:	n/a	n/a
26	BHLHE40	chr11:9984365-9984604	GM12878	blood:	n/a	n/a
27	BRCA1	chr11:9927489-9928472	Hela-S3	cervix:	n/a	n/a
28	BRCA1	chr11:9994495-9994970	H1-hESC	embryonic stem cell:	n/a	n/a
29	CBX3	chr11:9921638-9922217	HCT-116	colon:	n/a	n/a
30	CBX3	chr11:9927406-9928048	HCT-116	colon:	n/a	chr11:9927755-9927766
31	CBX3	chr11:10004722-10005080	K562	blood:	n/a	n/a
32	CEBPB	chr11:9952541-9952703	K562	blood:	n/a	n/a
33	CEBPB	chr11:9927510-9928503	A549	lung:	n/a	chr11:9928085-9928096 chr11:9928087-9928098 chr11:9928085-9928098 chr11:9928085-9928098 chr11:9928087-9928098
34	CEBPB	chr11:9954472-9954738	HepG2	liver:	n/a	chr11:9954537-9954548
35	CEBPB	chr11:9965293-9965650	HepG2	liver:	n/a	n/a
36	CEBPB	chr11:9994600-9994759	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr11:9978063-9978347	K562	blood:	n/a	chr11:9978174-9978185
38	CEBPB	chr11:9965150-9965713	A549	lung:	n/a	n/a
39	CEBPB	chr11:9927557-9928292	IMR90	lung:	n/a	chr11:9928085-9928096 chr11:9928087-9928098 chr11:9928085-9928098 chr11:9928085-9928098 chr11:9928087-9928098
40	CEBPB	chr11:9927524-9928511	MCF-7	breast:	n/a	chr11:9928085-9928096 chr11:9928087-9928098 chr11:9928085-9928098 chr11:9928085-9928098 chr11:9928087-9928098
41	CEBPB	chr11:9923573-9923645	Hela-S3	cervix:	n/a	chr11:9923594-9923605
42	CEBPB	chr11:9965223-9965725	A549	lung:	n/a	n/a
43	CEBPB	chr11:9952475-9952674	HepG2	liver:	n/a	n/a
44	CEBPB	chr11:9928021-9928241	HepG2	liver:	n/a	chr11:9928085-9928096 chr11:9928087-9928098 chr11:9928085-9928098 chr11:9928085-9928098 chr11:9928087-9928098
45	CEBPB	chr11:9949280-9949580	HepG2	liver:	n/a	chr11:9949428-9949439
46	CEBPB	chr11:9990638-9990986	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr11:9964979-9965792	IMR90	lung:	n/a	n/a
48	CEBPB	chr11:9978058-9978263	IMR90	lung:	n/a	chr11:9978174-9978185
49	CEBPB	chr11:9927550-9928391	A549	lung:	n/a	chr11:9928085-9928096 chr11:9928087-9928098 chr11:9928085-9928098 chr11:9928085-9928098 chr11:9928087-9928098
50	CEBPB	chr11:9927352-9928483	Hela-S3	cervix:	n/a	chr11:9928085-9928096 chr11:9928087-9928098 chr11:9928085-9928098 chr11:9928085-9928098 chr11:9928087-9928098

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:9995602-9995652	GM06990	blood:	n/a
2	chr11:9944707-9944757	HCPEpiC	choroid plexus:	n/a
3	chr11:10002835-10002885	Jurkat	blood:	n/a
4	chr11:9995602-9995652	AG10803	skin:	n/a
5	chr11:9995602-9995652	GM19239	blood:	n/a
6	chr11:10002835-10002885	HRE	kidney:	n/a
7	chr11:10002835-10002885	A549	lung:	n/a
8	chr11:10002835-10002885	HRCEpiC	kidney:	n/a
9	chr11:10002835-10002885	AG09309	skin:	n/a
10	chr11:9995602-9995652	CMK	blood:	n/a
11	chr11:9995602-9995652	NHDF-neo	bronchial:	n/a
12	chr11:9995602-9995652	HEK293	kidney:	embryo
13	chr11:9944707-9944757	SK-N-SH	brain:	n/a
14	chr11:9944707-9944757	HEEpiC	esophagus:	n/a
15	chr11:9995602-9995652	HL-60	blood:	n/a
16	chr11:10002835-10002885	PrEC	prostate:	n/a
17	chr11:9992187-9992237	LNCaP	prostate:	n/a
18	chr11:10002835-10002885	Caco-2	colon:	n/a
19	chr11:9944707-9944757	MCF10A-Er-Src	breast:	n/a
20	chr11:10002835-10002885	NHDF-neo	bronchial:	n/a
21	chr11:9992187-9992237	ovcar-3	ovarian:	n/a
22	chr11:9995602-9995652	GM12892	blood:	n/a
23	chr11:9992187-9992237	IMR90	lung:	fetal
24	chr11:10002835-10002885	HEEpiC	esophagus:	n/a
25	chr11:9915200-9915250	A549	lung:	n/a
26	chr11:10002835-10002885	ovcar-3	ovarian:	n/a
27	chr11:10002835-10002885	PFSK-1	brain:	n/a
28	chr11:10002835-10002885	HCPEpiC	choroid plexus:	n/a
29	chr11:9915200-9915250	HepG2	liver:	n/a
30	chr11:10002835-10002885	HRPEpiC	eye:	n/a
31	chr11:9995602-9995652	SK-N-MC	brain:	n/a
32	chr11:9992187-9992237	NHDF-neo	bronchial:	n/a
33	chr11:10002835-10002885	MCF10A-Er-Src	breast:	n/a
34	chr11:9992187-9992237	HNPCEpiC	eye:	n/a
35	chr11:9944707-9944757	HUVEC	blood vessel:	n/a
36	chr11:10002835-10002885	LNCaP	prostate:	n/a
37	chr11:9995602-9995652	K562	blood:	n/a
38	chr11:9995602-9995652	Hepatocyte	liver:	n/a
39	chr11:9915200-9915250	Jurkat	blood:	n/a
40	chr11:9992187-9992237	Hela-S3	cervix:	n/a
41	chr11:9944707-9944757	IMR90	lung:	fetal
42	chr11:9995602-9995652	HCM	heart:	n/a
43	chr11:9995602-9995652	HUVEC	blood vessel:	n/a
44	chr11:9915200-9915250	HMEC	breast:	n/a
45	chr11:9915200-9915250	NB4	blood:	n/a
46	chr11:9995602-9995652	HAEpiC	amniotic membrane:	n/a
47	chr11:9944707-9944757	HL-60	blood:	n/a
48	chr11:9944707-9944757	Caco-2	colon:	n/a
49	chr11:9995602-9995652	HRE	kidney:	n/a
50	chr11:9992187-9992237	CMK	blood:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:9928185..9930607-chr11:9931281..9933826,2	MCF-7	breast:
2	chr11:10002720..10004321-chr11:10011527..10014066,2	K562	blood:
3	chr11:9926975..9929844-chr11:10324322..10328573,4	MCF-7	breast:
4	chr11:9918384..9921801-chr11:9925480..9929741,5	MCF-7	breast:
5	chr11:9991428..9993143-chr11:10058135..10060614,2	K562	blood:
6	chr11:9926719..9929001-chr11:10324531..10327507,2	MCF-7	breast:
7	chr11:9883380..9884276-chr11:9994232..9995105,4	MCF-7	breast:
8	chr11:10012021..10012653-chr11:10098365..10099087,2	MCF-7	breast:
9	chr11:9928185..9930607-chr11:9931281..9933826,2	MCF-7	breast:
10	chr11:9482450..9484248-chr11:9984519..9986171,2	K562	blood:
11	chr11:10004750..10006557-chr11:10010668..10012877,2	MCF-7	breast:
12	chr11:10011394..10012992-chr11:10327878..10330326,2	MCF-7	breast:
13	chr11:9883445..9884416-chr11:9994096..9994928,3	MCF-7	breast:
14	chr11:9994842..9997807-chr11:10313418..10316499,3	MCF-7	breast:
15	chr11:9918384..9921801-chr11:9925480..9929741,5	MCF-7	breast:
16	chr11:9994901..9996412-chr11:10324131..10325757,2	MCF-7	breast:
17	chr11:10004750..10006557-chr11:10010668..10012877,2	MCF-7	breast:
18	chr11:10010659..10013525-chr11:10017615..10019134,2	K562	blood:
19	chr11:9967314..9969682-chr11:9973855..9976394,2	MCF-7	breast:
20	chr11:9779414..9780281-chr11:9994114..9995162,4	K562	blood:
21	chr11:10002720..10004321-chr11:10011527..10014066,2	K562	blood:
22	chr11:10000703..10003036-chr11:10327811..10330632,2	MCF-7	breast:
23	chr11:9967314..9969682-chr11:9973855..9976394,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SWAP70-2	chr11:9950437-9950810	ENSG00000255476.1
2	lnc-SWAP70-2	chr11:9937153-9937230	ENSG00000255476.1

No data

Variant related genes	Relation type
ENSG00000254765	TF binding region
SBF2	TF binding region
ENSG00000254765	CpG island
SBF2	CpG island
ENSG00000133812	chromatin interactions
ENSG00000148926	chromatin interactions
ENSG00000133805	chromatin interactions
ENSG00000245522	chromatin interactions
ENSG00000246273	chromatin interactions
ENSG00000166478	chromatin interactions
ENSG00000254554	chromatin interactions

Extended variants
information (count: 4236 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:4236 , 50 per page) page: 1 2 3 4 5 6 7 ... 85

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10743120	chr11:9912052-9912053	Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs184351953	chr11:9912069-9912070	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs542926253	chr11:9912089-9912090	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs554096098	chr11:9912102-9912103	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs10840316	chr11:9912131-9912132	Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs530934206	chr11:9912171-9912172	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs537084511	chr11:9912185-9912186	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs73418583	chr11:9912200-9912201	Weak transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs144926047	chr11:9912230-9912231	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs189313140	chr11:9912276-9912277	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs546910626	chr11:9912297-9912298	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs6483792	chr11:9912310-9912311	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs529531948	chr11:9912338-9912339	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs373811624	chr11:9912352-9912353	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs549654680	chr11:9912403-9912404	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs367598281	chr11:9912408-9912409	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs182303104	chr11:9912423-9912424	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs545611373	chr11:9912446-9912447	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs35356095	chr11:9912468-9912469	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs79793595	chr11:9912493-9912494	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs186031429	chr11:9912517-9912518	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs57233768	chr11:9912518-9912519	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs141300784	chr11:9912521-9912522	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs189296331	chr11:9912543-9912544	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs180995083	chr11:9912568-9912569	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs542513398	chr11:9912668-9912669	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs556536648	chr11:9912703-9912704	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs575704312	chr11:9912746-9912747	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs542759506	chr11:9912755-9912756	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs544644753	chr11:9912773-9912774	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs185576631	chr11:9912774-9912775	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs116477577	chr11:9912777-9912778	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs533234680	chr11:9912781-9912782	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs150774402	chr11:9912786-9912787	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs138016777	chr11:9912807-9912808	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs143547748	chr11:9912821-9912822	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs547563498	chr11:9912885-9912886	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs117955090	chr11:9913010-9913011	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs190249763	chr11:9913038-9913039	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs183019504	chr11:9913049-9913050	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs566943376	chr11:9913089-9913090	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs186243612	chr11:9913095-9913096	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs531188115	chr11:9913097-9913098	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs572732357	chr11:9913101-9913102	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs192220129	chr11:9913119-9913120	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs147160885	chr11:9913157-9913158	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs184007821	chr11:9913172-9913173	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs372356837	chr11:9913289-9913290	Weak transcription Active TSS Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs12295264	chr11:9913338-9913339	Weak transcription Active TSS Enhancers Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs541766205	chr11:9913379-9913380	Weak transcription Active TSS Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Neuroblastoma	18923191	CNVD
Breast cancer	19432969	CNVD
Alzheimer''s disease	17576883	CNVD
Long-qt syndrome	17576883	CNVD
Emphysema	19352772	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Chordoma	18071362	CNVD
Breast cancer	16608533	CNVD
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
Autism	22495311	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Myelofibrosis	22110671	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Neuroblastoma	21124317	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Schizophrenia	21399695	CNVD
Gastric cancer	16891809	CNVD
Cancer	17160897	CNVD
Multiple myeloma	16616336	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1822 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:9878400-9916200	Weak transcription	Rectal Mucosa Donor 29	rectum
2	chr11:9878800-9952200	Weak transcription	Aorta	Aorta
3	chr11:9880200-9913200	Weak transcription	Monocytes-CD14+_RO01746	blood
4	chr11:9880600-9914800	Weak transcription	Placenta	Placenta
5	chr11:9882400-9929600	Weak transcription	Primary T cells from cord blood	blood
6	chr11:9890600-9915200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr11:9891400-9916800	Weak transcription	Primary B cells from cord blood	blood
8	chr11:9891800-9916600	Weak transcription	Duodenum Smooth Muscle	Duodenum
9	chr11:9892200-9914600	Weak transcription	Cortex derived primary cultured neurospheres	brain
10	chr11:9892400-9914400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr11:9892400-9914600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
12	chr11:9892400-9921200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr11:9894200-9915200	Weak transcription	Fetal Muscle Trunk	muscle
14	chr11:9894400-9916600	Weak transcription	Primary hematopoietic stem cells	blood
15	chr11:9894400-9978600	Weak transcription	Left Ventricle	heart
16	chr11:9897000-9915000	Weak transcription	HSMMtube	muscle
17	chr11:9898200-9914800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr11:9898200-9917000	Weak transcription	Stomach Smooth Muscle	stomach
19	chr11:9898400-9913800	Weak transcription	Fetal Stomach	stomach
20	chr11:9898600-9914800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
21	chr11:9898800-9915200	Weak transcription	Fetal Intestine Small	intestine
22	chr11:9899400-9915000	Weak transcription	Liver	Liver
23	chr11:9900600-9915000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
24	chr11:9901200-9915000	Weak transcription	H1 Cell Line	embryonic stem cell
25	chr11:9901200-9916600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr11:9902200-9917400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr11:9902400-9913000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr11:9903400-9915000	Weak transcription	Fetal Muscle Leg	muscle
29	chr11:9903600-9915200	Weak transcription	Ovary	ovary
30	chr11:9903600-9916600	Weak transcription	Fetal Lung	lung
31	chr11:9903800-9914600	Weak transcription	Primary monocytes fromperipheralblood	blood
32	chr11:9904000-9937000	Weak transcription	Sigmoid Colon	Sigmoid Colon
33	chr11:9906000-9915000	Weak transcription	Fetal Intestine Large	intestine
34	chr11:9906400-9912800	Weak transcription	NHLF	lung
35	chr11:9906400-9914800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr11:9906400-9915000	Weak transcription	Osteobl	bone
37	chr11:9906800-9920400	Weak transcription	HUVEC	blood vessel
38	chr11:9907000-9914800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
39	chr11:9908400-9915000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr11:9909200-9915000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr11:9909400-9915000	Weak transcription	HUES6 Cell Line	embryonic stem cell
42	chr11:9909400-9916800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr11:9909600-9914800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr11:9909800-9916600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr11:9910000-9954600	Weak transcription	Pancreas	Pancrea
46	chr11:9910200-9921000	Weak transcription	Placenta Amnion	Placenta Amnion
47	chr11:9910800-9914600	Weak transcription	H9 Cell Line	embryonic stem cell
48	chr11:9910800-9915000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
49	chr11:9910800-9915000	Weak transcription	HSMM	muscle
50	chr11:9911000-9914800	Weak transcription	HUES48 Cell Line	embryonic stem cell

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