Variant report

Variant	nsv1037131
Chromosome Location	chr11:10401998-10429998
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:721)
CpG islands
(count:244)
Chromatin interactive
region (count:21)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:721 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:10416170-10416381	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:10427623-10427993	K562	blood:	n/a	n/a
3	ARID3A	chr11:10427690-10428034	HepG2	liver:	n/a	n/a
4	ATF1	chr11:10427721-10428057	K562	blood:	n/a	n/a
5	ATF1	chr11:10428531-10428836	K562	blood:	n/a	n/a
6	ATF2	chr11:10427584-10428087	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr11:10427476-10428112	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr11:10415795-10416789	A549	lung:	n/a	n/a
9	ATF3	chr11:10427678-10428055	K562	blood:	n/a	n/a
10	ATF3	chr11:10415972-10416702	A549	lung:	n/a	n/a
11	BACH1	chr11:10427632-10428122	K562	blood:	n/a	n/a
12	BACH1	chr11:10427668-10428146	H1-hESC	embryonic stem cell:	n/a	n/a
13	BATF	chr11:10427779-10428076	GM12878	blood:	n/a	n/a
14	BCL3	chr11:10416011-10416772	A549	lung:	n/a	n/a
15	BCL3	chr11:10415827-10416866	A549	lung:	n/a	n/a
16	BHLHE40	chr11:10420060-10420390	K562	blood:	n/a	n/a
17	BHLHE40	chr11:10409105-10409183	K562	blood:	n/a	n/a
18	BHLHE40	chr11:10428563-10429003	K562	blood:	n/a	n/a
19	BHLHE40	chr11:10415949-10416571	A549	lung:	n/a	n/a
20	BHLHE40	chr11:10414416-10414595	K562	blood:	n/a	chr11:10414507-10414520 chr11:10414509-10414518 chr11:10414509-10414518
21	BHLHE40	chr11:10416071-10416459	HepG2	liver:	n/a	n/a
22	BHLHE40	chr11:10427800-10428059	K562	blood:	n/a	n/a
23	BHLHE40	chr11:10427709-10428016	GM12878	blood:	n/a	n/a
24	BRCA1	chr11:10428471-10428867	Hela-S3	cervix:	n/a	n/a
25	BRCA1	chr11:10428716-10428744	GM12878	blood:	n/a	n/a
26	BRCA1	chr11:10427709-10428064	Hela-S3	cervix:	n/a	n/a
27	BRCA1	chr11:10420917-10421015	HepG2	liver:	n/a	n/a
28	CBX3	chr11:10427633-10428124	K562	blood:	n/a	n/a
29	CCNT2	chr11:10428561-10428785	K562	blood:	n/a	n/a
30	CEBPB	chr11:10427718-10428048	A549	lung:	n/a	chr11:10427770-10427781
31	CEBPB	chr11:10428595-10428790	A549	lung:	n/a	n/a
32	CEBPB	chr11:10415975-10416827	A549	lung:	n/a	n/a
33	CEBPB	chr11:10427706-10427973	HepG2	liver:	n/a	chr11:10427770-10427781
34	CEBPB	chr11:10427629-10428001	IMR90	lung:	n/a	chr11:10427770-10427781
35	CEBPB	chr11:10416164-10416668	A549	lung:	n/a	n/a
36	CEBPB	chr11:10416408-10416536	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr11:10416211-10416638	IMR90	lung:	n/a	n/a
38	CEBPB	chr11:10428481-10428944	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr11:10416143-10416656	A549	lung:	n/a	n/a
40	CEBPB	chr11:10427647-10428045	K562	blood:	n/a	chr11:10427770-10427781
41	CEBPB	chr11:10427736-10428035	K562	blood:	n/a	chr11:10427770-10427781
42	CEBPB	chr11:10427678-10428003	A549	lung:	n/a	chr11:10427770-10427781
43	CEBPB	chr11:10427680-10428054	Hela-S3	cervix:	n/a	chr11:10427770-10427781
44	CEBPB	chr11:10408558-10409277	IMR90	lung:	n/a	n/a
45	CEBPB	chr11:10427674-10427989	H1-hESC	embryonic stem cell:	n/a	chr11:10427770-10427781
46	CEBPB	chr11:10408724-10408875	HepG2	liver:	n/a	n/a
47	CEBPD	chr11:10428407-10428939	K562	blood:	n/a	n/a
48	CEBPD	chr11:10428491-10428859	K562	blood:	n/a	n/a
49	CHD1	chr11:10427699-10427740	GM12878	blood:	n/a	n/a
50	CHD2	chr11:10428579-10428899	Hela-S3	cervix:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:10416227-10416277	U87	brain:	n/a
2	chr11:10427964-10428014	SAEC	small airway:	n/a
3	chr11:10429980-10430030	Hepatocyte	liver:	n/a
4	chr11:10427964-10428014	ECC-1	luminal epithelium:	n/a
5	chr11:10427964-10428014	NHDF-neo	bronchial:	n/a
6	chr11:10408528-10408578	HPAEpiC	pulmonary alveolar:	n/a
7	chr11:10416227-10416277	HCT-116	colon:	n/a
8	chr11:10416227-10416277	Hepatocyte	liver:	n/a
9	chr11:10429980-10430030	HPAEpiC	pulmonary alveolar:	n/a
10	chr11:10427964-10428014	NB4	blood:	n/a
11	chr11:10416227-10416277	HAEpiC	amniotic membrane:	n/a
12	chr11:10429980-10430030	HRCEpiC	kidney:	n/a
13	chr11:10408528-10408578	ovcar-3	ovarian:	n/a
14	chr11:10408528-10408578	PFSK-1	brain:	n/a
15	chr11:10416227-10416277	HCF	heart:	n/a
16	chr11:10429980-10430030	MCF-7	breast:	n/a
17	chr11:10427964-10428014	GM06990	blood:	n/a
18	chr11:10408528-10408578	SK-N-SH_RA	brain:	n/a
19	chr11:10427964-10428014	LNCaP	prostate:	n/a
20	chr11:10416227-10416277	HIPEpiC	eye:	n/a
21	chr11:10427964-10428014	HPAEpiC	pulmonary alveolar:	n/a
22	chr11:10408528-10408578	GM12892	blood:	n/a
23	chr11:10429980-10430030	HCM	heart:	n/a
24	chr11:10429980-10430030	HNPCEpiC	eye:	n/a
25	chr11:10429980-10430030	HRE	kidney:	n/a
26	chr11:10408528-10408578	H1-hESC	embryonic stem cell:	embryo
27	chr11:10429980-10430030	HEK293	kidney:	embryo
28	chr11:10427964-10428014	HRPEpiC	eye:	n/a
29	chr11:10408528-10408578	AoSMC	blood vessel:	n/a
30	chr11:10427964-10428014	HUVEC	blood vessel:	n/a
31	chr11:10416227-10416277	GM19239	blood:	n/a
32	chr11:10408528-10408578	HCT-116	colon:	n/a
33	chr11:10429980-10430030	HCF	heart:	n/a
34	chr11:10408528-10408578	LNCaP	prostate:	n/a
35	chr11:10427964-10428014	HNPCEpiC	eye:	n/a
36	chr11:10429980-10430030	HMEC	breast:	n/a
37	chr11:10408528-10408578	HNPCEpiC	eye:	n/a
38	chr11:10427964-10428014	MCF-7	breast:	n/a
39	chr11:10408528-10408578	U87	brain:	n/a
40	chr11:10416227-10416277	HPAEpiC	pulmonary alveolar:	n/a
41	chr11:10429980-10430030	NHBE	bronchial:	n/a
42	chr11:10429980-10430030	RPTEC	kidney:	n/a
43	chr11:10427964-10428014	PANC-1	pancreas:	n/a
44	chr11:10416227-10416277	A549	lung:	n/a
45	chr11:10427964-10428014	MCF10A-Er-Src	breast:	n/a
46	chr11:10427964-10428014	HEK293	kidney:	embryo
47	chr11:10427964-10428014	AG09319	gingival:	n/a
48	chr11:10408528-10408578	K562	blood:	n/a
49	chr11:10408528-10408578	HCF	heart:	n/a
50	chr11:10408528-10408578	HepG2	liver:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:10419157..10420679-chr11:10421309..10424308,2	MCF-7	breast:
2	chr11:10427450..10428226-chr11:10535022..10536041,3	MCF-7	breast:
3	chr11:10322917..10326761-chr11:10411066..10413981,3	MCF-7	breast:
4	chr11:10427821..10428361-chr11:10562807..10563319,2	K562	blood:
5	chr11:10419157..10420679-chr11:10421309..10424308,2	MCF-7	breast:
6	chr11:10387938..10388816-chr11:10427798..10428324,2	MCF-7	breast:
7	chr11:10414737..10416495-chr11:10419246..10421042,2	MCF-7	breast:
8	chr11:10427808..10432250-chr11:10475440..10478017,5	K562	blood:
9	chr11:10427811..10428324-chr11:10675560..10676361,2	MCF-7	breast:
10	chr11:10428535..10430173-chr11:10471249..10473167,2	MCF-7	breast:
11	chr11:10408455..10411116-chr11:10414237..10415892,3	MCF-7	breast:
12	chr11:10408455..10411116-chr11:10414237..10415892,3	MCF-7	breast:
13	chr11:10325849..10328171-chr11:10416407..10418101,2	MCF-7	breast:
14	chr11:10427762..10428619-chr11:10675503..10676394,3	K562	blood:
15	chr11:10410521..10412872-chr11:10414972..10416524,2	K562	blood:
16	chr11:10410521..10412872-chr11:10414972..10416524,2	K562	blood:
17	chr11:10423702..10425304-chr11:10426286..10427844,2	MCF-7	breast:
18	chr11:10427758..10428669-chr11:10756932..10757785,3	MCF-7	breast:
19	chr11:10427272..10428747-chr11:10756868..10757977,15	K562	blood:
20	chr11:10423702..10425304-chr11:10426286..10427844,2	MCF-7	breast:
21	chr11:10388047..10388889-chr11:10408886..10409883,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AMPD3-2	chr11:10413830-10413952	NONHSAT017964
2	lnc-AMPD3-2	chr11:10429915-10430052	NONHSAT017967
3	lnc-AMPD3-2	chr11:10413829-10413952	NONHSAT017963

No data

Variant related genes	Relation type
AMPD3	TF binding region
RNU6ATAC33P	TF binding region
AMPD3	CpG island
RNU6ATAC33P	CpG island
ENSG00000148926	chromatin interactions
ENSG00000221574	chromatin interactions
ENSG00000133805	chromatin interactions
ENSG00000177112	chromatin interactions
ENSG00000254554	chromatin interactions

Extended variants
information (count: 1213 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:1213 , 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	rs527474631	chr11:10402008-10402009	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs547336260	chr11:10402072-10402073	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs188204065	chr11:10402101-10402102	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs562315643	chr11:10402138-10402139	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs376483897	chr11:10402160-10402161	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs192797314	chr11:10402180-10402181	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs555757245	chr11:10402192-10402193	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs568884423	chr11:10402223-10402224	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs537983622	chr11:10402226-10402227	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs558222951	chr11:10402243-10402244	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs578143706	chr11:10402299-10402300	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs540823104	chr11:10402303-10402304	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs368940579	chr11:10402381-10402382	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs554365009	chr11:10402399-10402400	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs574399748	chr11:10402415-10402416	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs543312684	chr11:10402443-10402444	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs149226580	chr11:10402501-10402502	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs531317496	chr11:10402505-10402506	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs116778546	chr11:10402604-10402605	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs564991768	chr11:10402656-10402657	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs185245506	chr11:10402672-10402673	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs143431865	chr11:10402676-10402677	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs7112833	chr11:10402685-10402686	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs147985920	chr11:10402691-10402692	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs10770108	chr11:10402694-10402695	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs7126751	chr11:10402726-10402727	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs538235129	chr11:10402756-10402757	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs140756304	chr11:10402779-10402780	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs571722185	chr11:10402795-10402796	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs189824707	chr11:10402805-10402806	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs145875178	chr11:10402859-10402860	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs138773239	chr11:10402919-10402920	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs543373574	chr11:10402924-10402925	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs540127654	chr11:10402949-10402950	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs556889729	chr11:10402952-10402953	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs576003457	chr11:10402971-10402972	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs544993900	chr11:10402983-10402984	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs2957666	chr11:10402988-10402989	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs386750603	chr11:10402992-10402993	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs7130885	chr11:10402993-10402994	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs560777112	chr11:10403090-10403091	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs569287824	chr11:10403095-10403096	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs529824553	chr11:10403128-10403129	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs147412187	chr11:10403145-10403146	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs563602298	chr11:10403165-10403166	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs72854762	chr11:10403313-10403314	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs551766634	chr11:10403361-10403362	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs571521634	chr11:10403438-10403439	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs534314749	chr11:10403499-10403500	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs2198010	chr11:10403539-10403540	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:64)

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
T-cell prolymphocytic leukemia	17713554	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:669 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:10391800-10403800	Enhancers	Adipose Nuclei	Adipose
2	chr11:10392800-10403000	Enhancers	NHLF	lung
3	chr11:10394600-10402200	Enhancers	NHDF-Ad	bronchial
4	chr11:10394600-10403000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr11:10398000-10403800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr11:10398000-10404000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr11:10398000-10404000	Enhancers	Osteobl	bone
8	chr11:10398600-10403200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr11:10399400-10403200	Weak transcription	Primary monocytes fromperipheralblood	blood
10	chr11:10399400-10403800	Weak transcription	Monocytes-CD14+_RO01746	blood
11	chr11:10399800-10402800	Enhancers	HSMMtube	muscle
12	chr11:10400000-10403000	Enhancers	Muscle Satellite Cultured Cells	--
13	chr11:10400600-10407200	Weak transcription	Ovary	ovary
14	chr11:10401000-10403000	Enhancers	HSMM	muscle
15	chr11:10401200-10402200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr11:10401400-10402000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr11:10401400-10402000	Enhancers	Duodenum Smooth Muscle	Duodenum
18	chr11:10401400-10402000	Enhancers	Esophagus	oesophagus
19	chr11:10401400-10402000	Enhancers	Fetal Stomach	stomach
20	chr11:10401400-10402000	Enhancers	Left Ventricle	heart
21	chr11:10401400-10402000	Enhancers	Stomach Smooth Muscle	stomach
22	chr11:10401400-10402200	Enhancers	Breast Myoepithelial Primary Cells	Breast
23	chr11:10401600-10402000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr11:10401600-10402000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr11:10401600-10402000	Enhancers	Colon Smooth Muscle	Colon
26	chr11:10401600-10402200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr11:10401600-10402800	Enhancers	Right Atrium	heart
28	chr11:10401800-10407200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr11:10401800-10407200	Weak transcription	Fetal Muscle Leg	muscle
30	chr11:10401800-10407200	Weak transcription	Lung	lung
31	chr11:10401800-10407200	Weak transcription	Skeletal Muscle Male	skeletal muscle
32	chr11:10402000-10402600	Weak transcription	Esophagus	oesophagus
33	chr11:10402000-10404600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr11:10402000-10407200	Weak transcription	Colon Smooth Muscle	Colon
35	chr11:10402000-10407200	Weak transcription	Duodenum Smooth Muscle	Duodenum
36	chr11:10402000-10407200	Weak transcription	Stomach Smooth Muscle	stomach
37	chr11:10402200-10407200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr11:10402200-10407200	Weak transcription	NHDF-Ad	bronchial
39	chr11:10402600-10402800	Enhancers	Esophagus	oesophagus
40	chr11:10402800-10403000	Weak transcription	Right Atrium	heart
41	chr11:10402800-10408400	Weak transcription	Esophagus	oesophagus
42	chr11:10403000-10403400	Weak transcription	Muscle Satellite Cultured Cells	--
43	chr11:10403000-10407200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr11:10403200-10403400	Enhancers	Primary monocytes fromperipheralblood	blood
45	chr11:10403200-10403400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr11:10403400-10404000	Enhancers	Muscle Satellite Cultured Cells	--
47	chr11:10403400-10404200	Weak transcription	Primary monocytes fromperipheralblood	blood
48	chr11:10403400-10408400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr11:10403800-10404600	Enhancers	Monocytes-CD14+_RO01746	blood
50	chr11:10403800-10407200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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