Variant report

Variant	nsv75
Chromosome Location	chr11:107219624-107251780
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	ATF1	chr11:107240708-107240809	K562	blood:	n/a	n/a
2	ATF2	chr11:107241054-107241483	GM12878	blood:	n/a	n/a
3	CTCF	chr11:107244188-107244259	GM10248	blood:	n/a	n/a
4	CTCF	chr11:107233572-107233629	Kidney_OC	kidney:	n/a	n/a
5	EBF1	chr11:107241262-107241305	GM12878	blood:	n/a	n/a
6	FOS	chr11:107241124-107241415	HUVEC	blood vessel:	n/a	chr11:107241238-107241247 chr11:107241234-107241245 chr11:107241236-107241248 chr11:107241239-107241246 chr11:107241236-107241247 chr11:107241237-107241247 chr11:107241238-107241246
7	FOS	chr11:107222374-107222525	MCF10A-Er-Src	breast:	n/a	n/a
8	FOS	chr11:107241026-107241427	MCF10A-Er-Src	breast:	n/a	chr11:107241238-107241247 chr11:107241234-107241245 chr11:107241236-107241248 chr11:107241239-107241246 chr11:107241236-107241247 chr11:107241237-107241247 chr11:107241238-107241246
9	FOS	chr11:107241009-107241427	MCF10A-Er-Src	breast:	n/a	chr11:107241238-107241247 chr11:107241234-107241245 chr11:107241236-107241248 chr11:107241239-107241246 chr11:107241236-107241247 chr11:107241237-107241247 chr11:107241238-107241246
10	FOS	chr11:107241063-107241412	MCF10A-Er-Src	breast:	n/a	chr11:107241238-107241247 chr11:107241234-107241245 chr11:107241236-107241248 chr11:107241239-107241246 chr11:107241236-107241247 chr11:107241237-107241247 chr11:107241238-107241246
11	FOS	chr11:107241068-107241494	MCF10A-Er-Src	breast:	n/a	chr11:107241238-107241247 chr11:107241234-107241245 chr11:107241236-107241248 chr11:107241239-107241246 chr11:107241236-107241247 chr11:107241237-107241247 chr11:107241238-107241246
12	FOSL2	chr11:107241093-107241436	SK-N-SH	brain:	n/a	chr11:107241238-107241247 chr11:107241234-107241245 chr11:107241236-107241248 chr11:107241239-107241246 chr11:107241237-107241247 chr11:107241238-107241246
13	FOXA1	chr11:107240572-107241011	HepG2	liver:	n/a	n/a
14	FOXA1	chr11:107240552-107240908	HepG2	liver:	n/a	n/a
15	FOXA1	chr11:107243732-107244134	HepG2	liver:	n/a	n/a
16	FOXA2	chr11:107232651-107233340	A549	lung:	n/a	n/a
17	FOXA2	chr11:107243578-107244314	A549	lung:	n/a	n/a
18	FOXA2	chr11:107240625-107240831	HepG2	liver:	n/a	n/a
19	GATA3	chr11:107228678-107228906	SH-SY5Y	brain:	n/a	n/a
20	GATA3	chr11:107231469-107231532	SH-SY5Y	brain:	n/a	n/a
21	IKZF1	chr11:107241166-107241438	GM12878	blood:	n/a	n/a
22	JUN	chr11:107224358-107224368	H1-hESC	embryonic stem cell:	n/a	n/a
23	JUND	chr11:107222361-107222588	K562	blood:	n/a	n/a
24	MEF2A	chr11:107241201-107241533	GM12878	blood:	n/a	chr11:107241384-107241405 chr11:107241388-107241404 chr11:107241391-107241400 chr11:107241390-107241401 chr11:107241389-107241403 chr11:107241384-107241405
25	MEF2C	chr11:107241165-107241511	GM12878	blood:	n/a	chr11:107241384-107241405 chr11:107241388-107241404 chr11:107241391-107241400 chr11:107241390-107241401 chr11:107241389-107241403 chr11:107241384-107241405
26	MYC	chr11:107241180-107241393	MCF10A-Er-Src	breast:	n/a	chr11:107241237-107241246 chr11:107241238-107241247
27	NFIC	chr11:107240993-107241433	GM12878	blood:	n/a	n/a
28	NFYB	chr11:107229613-107229700	GM12878	blood:	n/a	n/a
29	POLR2A	chr11:107232783-107233017	H1-hESC	embryonic stem cell:	n/a	n/a
30	POLR2A	chr11:107231607-107231731	MCF10A-Er-Src	breast:	n/a	n/a
31	POLR2A	chr11:107243779-107243982	H1-hESC	embryonic stem cell:	n/a	n/a
32	POLR2A	chr11:107232159-107232356	MCF10A-Er-Src	breast:	n/a	n/a
33	POLR2A	chr11:107219760-107219777	MCF10A-Er-Src	breast:	n/a	n/a
34	POLR2A	chr11:107243279-107244215	H1-hESC	embryonic stem cell:	n/a	n/a
35	POLR2A	chr11:107243240-107243312	H1-hESC	embryonic stem cell:	n/a	n/a
36	POLR2A	chr11:107232837-107233153	H1-hESC	embryonic stem cell:	n/a	n/a
37	POLR2A	chr11:107232533-107233078	H1-hESC	embryonic stem cell:	n/a	n/a
38	POLR2A	chr11:107243748-107243995	H1-hESC	embryonic stem cell:	n/a	n/a
39	POLR2A	chr11:107228421-107228478	MCF10A-Er-Src	breast:	n/a	n/a
40	POLR2A	chr11:107243362-107244084	H1-hESC	embryonic stem cell:	n/a	n/a
41	POLR2A	chr11:107232831-107233008	H1-hESC	embryonic stem cell:	n/a	n/a
42	POLR2A	chr11:107243619-107244044	H1-hESC	embryonic stem cell:	n/a	n/a
43	POLR2A	chr11:107250916-107250939	MCF10A-Er-Src	breast:	n/a	n/a
44	POLR2A	chr11:107232820-107232834	H1-hESC	embryonic stem cell:	n/a	n/a
45	POLR2A	chr11:107243806-107243911	A549	lung:	n/a	n/a
46	RUNX3	chr11:107241168-107241529	GM12878	blood:	n/a	n/a
47	SRF	chr11:107232590-107232783	GM12878	blood:	n/a	n/a
48	STAT3	chr11:107241183-107241371	MCF10A-Er-Src	breast:	n/a	chr11:107241238-107241247 chr11:107241237-107241246
49	STAT3	chr11:107230844-107230852	MCF10A-Er-Src	breast:	n/a	n/a
50	STAT3	chr11:107243023-107243035	MCF10A-Er-Src	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:107243587-107243637	HIPEpiC	eye:	n/a
2	chr11:107243587-107243637	HIPEpiC	eye:	n/a
3	chr11:107243587-107243637	A549	lung:	n/a
4	chr11:107232729-107232779	SAEC	small airway:	n/a
5	chr11:107243587-107243637	CMK	blood:	n/a
6	chr11:107243587-107243637	NH-A	brain:	n/a
7	chr11:107232729-107232779	HCPEpiC	choroid plexus:	n/a
8	chr11:107232729-107232779	PFSK-1	brain:	n/a
9	chr11:107243587-107243637	AG04450	lung:	fetal
10	chr11:107243587-107243637	HCF	heart:	n/a
11	chr11:107243587-107243637	RPTEC	kidney:	n/a
12	chr11:107243587-107243637	HNPCEpiC	eye:	n/a
13	chr11:107243587-107243637	SAEC	small airway:	n/a
14	chr11:107243587-107243637	H1-hESC	embryonic stem cell:	embryo
15	chr11:107232729-107232779	GM19239	blood:	n/a
16	chr11:107243587-107243637	HPAEpiC	pulmonary alveolar:	n/a
17	chr11:107232729-107232779	GM12892	blood:	n/a
18	chr11:107243587-107243637	HL-60	blood:	n/a
19	chr11:107232729-107232779	MCF10A-Er-Src	breast:	n/a
20	chr11:107232729-107232779	SKMC	muscle:	n/a
21	chr11:107243587-107243637	T-47D	breast:	n/a
22	chr11:107232729-107232779	Caco-2	colon:	n/a
23	chr11:107243587-107243637	PANC-1	pancreas:	n/a
24	chr11:107243587-107243637	Hela-S3	cervix:	n/a
25	chr11:107232729-107232779	AoSMC	blood vessel:	n/a
26	chr11:107232729-107232779	Jurkat	blood:	n/a
27	chr11:107243587-107243637	HMEC	breast:	n/a
28	chr11:107243587-107243637	AG10803	skin:	n/a
29	chr11:107232729-107232779	HRE	kidney:	n/a
30	chr11:107232729-107232779	A549	lung:	n/a
31	chr11:107232729-107232779	AG04450	lung:	fetal
32	chr11:107232729-107232779	AG04449	skin:	fetal
33	chr11:107243587-107243637	U87	brain:	n/a
34	chr11:107243587-107243637	SK-N-SH	brain:	n/a
35	chr11:107243587-107243637	PFSK-1	brain:	n/a
36	chr11:107243587-107243637	GM12878	blood:	n/a
37	chr11:107243587-107243637	AoSMC	blood vessel:	n/a
38	chr11:107243587-107243637	ProgFib	skin:	n/a
39	chr11:107232729-107232779	PANC-1	pancreas:	n/a
40	chr11:107232729-107232779	NT2-D1	testis:	n/a
41	chr11:107232729-107232779	ovcar-3	ovarian:	n/a
42	chr11:107243587-107243637	NB4	blood:	n/a
43	chr11:107243587-107243637	SK-N-SH_RA	brain:	n/a
44	chr11:107243587-107243637	HCT-116	colon:	n/a
45	chr11:107232729-107232779	SK-N-MC	brain:	n/a
46	chr11:107243587-107243637	HCM	heart:	n/a
47	chr11:107232729-107232779	H1-hESC	embryonic stem cell:	embryo
48	chr11:107243587-107243637	HRPEpiC	eye:	n/a
49	chr11:107232729-107232779	NHBE	bronchial:	n/a
50	chr11:107243587-107243637	GM19239	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:107240491..107241393-chr16:2244600..2245300,2	MCF-7	breast:
2	chr11:107237489..107239255-chr11:107241546..107243344,2	K562	blood:
3	chr11:107216471..107218529-chr11:107219942..107221612,2	K562	blood:
4	chr11:107237489..107239255-chr11:107241546..107243344,2	K562	blood:
5	chr11:107215828..107218529-chr11:107218963..107221832,3	K562	blood:
6	chr11:107213050..107215630-chr11:107219007..107221031,2	K562	blood:
7	chr11:107241951..107244732-chr11:107327122..107328857,2	K562	blood:

Variant related genes	Relation type
CWF19L2	TF binding region
CWF19L2	CpG island
ENSG00000152404	chromatin interactions

Extended variants
information (count: 1235 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:1235 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs76315395	chr11:107219629-107219630	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs367861452	chr11:107219646-107219647	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs530758548	chr11:107219647-107219648	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs201724585	chr11:107219648-107219649	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs570771392	chr11:107219673-107219674	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs368279169	chr11:107219690-107219691	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs375063598	chr11:107219751-107219752	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs199671858	chr11:107219758-107219759	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs142799271	chr11:107219760-107219761	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs564621945	chr11:107219782-107219783	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs201962833	chr11:107219788-107219789	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs368434567	chr11:107219804-107219805	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs535089525	chr11:107219815-107219816	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs570058368	chr11:107219884-107219885	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs139973914	chr11:107219911-107219912	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs568824652	chr11:107219924-107219925	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs77648901	chr11:107219948-107219949	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs191774175	chr11:107219962-107219963	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs573097087	chr11:107220066-107220067	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs540562959	chr11:107220067-107220068	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs183177605	chr11:107220300-107220301	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs77829838	chr11:107220308-107220309	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs537070623	chr11:107220338-107220339	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs11421851	chr11:107220350-107220351	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs397740140	chr11:107220360-107220361	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs201613673	chr11:107220361-107220362	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs563017143	chr11:107220369-107220370	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs7129866	chr11:107220429-107220430	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs573449	chr11:107220459-107220460	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs534748989	chr11:107220470-107220471	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs58723152	chr11:107220551-107220552	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs546950386	chr11:107220571-107220572	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs368553517	chr11:107220595-107220596	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs77181355	chr11:107220596-107220597	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs528897301	chr11:107220612-107220613	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs117867081	chr11:107220613-107220614	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs188473553	chr11:107220616-107220617	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs539203531	chr11:107220685-107220686	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs146773354	chr11:107220714-107220715	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs111387453	chr11:107220749-107220750	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs537978557	chr11:107220790-107220791	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs566756029	chr11:107220828-107220829	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs192945058	chr11:107220862-107220863	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs185545761	chr11:107220865-107220866	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs189258108	chr11:107220949-107220950	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs371332622	chr11:107220964-107220965	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs375737977	chr11:107220976-107220977	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs544605504	chr11:107221026-107221027	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs60413796	chr11:107221037-107221038	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs577969082	chr11:107221082-107221083	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	20729466	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Cervical cancer	21062161	CNVD
Esophageal squamous carcinoma	18350619	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	22429812	CNVD
Breast cancer	16608533	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16785998	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21958427	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17603634	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Basal cell lymphoma	16790693	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21364760	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Mental retardation	19966786	CNVD
Non-small cell lung cancer	21829676	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Intracranial aneurysm	16715129	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Ovarian cancer	21720365	CNVD
Chronic lymphocytic leukemia	17805327	CNVD
Glioblastoma multiforme	22286061	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Neuroblastoma	17327916	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Mantle cell lymphoma	19029149	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant melanoma	17260012	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Obesity	19966786	CNVD
Renal cell carcinoma	21668985	CNVD
Cancer	20164920	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:299 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:107169400-107230000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
2	chr11:107173600-107231400	Weak transcription	Brain Angular Gyrus	brain
3	chr11:107179200-107229800	Weak transcription	Psoas Muscle	Psoas
4	chr11:107180000-107233200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
5	chr11:107183400-107234400	Weak transcription	HSMMtube	muscle
6	chr11:107190000-107223200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr11:107192000-107224200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr11:107192200-107223800	Weak transcription	Brain Substantia Nigra	brain
9	chr11:107192200-107225600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr11:107192200-107229000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr11:107192200-107232200	Weak transcription	Esophagus	oesophagus
12	chr11:107193800-107229800	Weak transcription	Right Ventricle	heart
13	chr11:107193800-107237200	Weak transcription	Gastric	stomach
14	chr11:107194600-107221200	Weak transcription	Rectal Smooth Muscle	rectum
15	chr11:107194600-107235600	Weak transcription	Aorta	Aorta
16	chr11:107194800-107221000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
17	chr11:107194800-107221600	Weak transcription	Brain Cingulate Gyrus	brain
18	chr11:107194800-107223000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr11:107194800-107224000	Weak transcription	Small Intestine	intestine
20	chr11:107195000-107223200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr11:107195000-107299200	Weak transcription	Colon Smooth Muscle	Colon
22	chr11:107195200-107222000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
23	chr11:107195200-107224000	Weak transcription	Thymus	Thymus
24	chr11:107195200-107225800	Weak transcription	HSMM	muscle
25	chr11:107195200-107233000	Weak transcription	Fetal Muscle Trunk	muscle
26	chr11:107195800-107220000	Weak transcription	HUES48 Cell Line	embryonic stem cell
27	chr11:107197000-107228200	Weak transcription	Fetal Stomach	stomach
28	chr11:107197800-107220800	Weak transcription	Rectal Mucosa Donor 31	rectum
29	chr11:107198200-107221200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
30	chr11:107198200-107233200	Weak transcription	Placenta	Placenta
31	chr11:107198200-107240800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr11:107198800-107221000	Weak transcription	Sigmoid Colon	Sigmoid Colon
33	chr11:107199400-107221200	Weak transcription	Fetal Intestine Large	intestine
34	chr11:107200200-107221400	Weak transcription	Brain Inferior Temporal Lobe	brain
35	chr11:107200400-107221400	Weak transcription	Stomach Smooth Muscle	stomach
36	chr11:107200800-107224400	Weak transcription	Fetal Thymus	thymus
37	chr11:107203000-107226200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
38	chr11:107204000-107227400	Weak transcription	Pancreas	Pancrea
39	chr11:107204800-107220800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr11:107205600-107234800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
41	chr11:107213200-107222200	Weak transcription	Colonic Mucosa	Colon
42	chr11:107214000-107222000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
43	chr11:107214200-107220800	Weak transcription	HUVEC	blood vessel
44	chr11:107214200-107225400	Weak transcription	Fetal Brain Female	brain
45	chr11:107214200-107232600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr11:107215400-107220800	Weak transcription	Rectal Mucosa Donor 29	rectum
47	chr11:107215400-107222400	Weak transcription	Brain Anterior Caudate	brain
48	chr11:107215400-107226200	Weak transcription	HepG2	liver
49	chr11:107215400-107231200	Weak transcription	Skeletal Muscle Male	skeletal muscle
50	chr11:107215600-107221000	Weak transcription	Fetal Lung	lung

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