Variant report

Variant	esv3347109
Chromosome Location	chr11:87163383-87245753
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	BCL11A	chr11:87204621-87204917	H1-hESC	embryonic stem cell:	n/a	n/a
2	BCL11A	chr11:87204640-87204899	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr11:87180842-87181077	HepG2	liver:	n/a	chr11:87180927-87180938 chr11:87180926-87180937 chr11:87180926-87180939 chr11:87180926-87180937
4	CEBPB	chr11:87177314-87177627	IMR90	lung:	n/a	n/a
5	CEBPB	chr11:87204666-87205419	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr11:87212560-87212680	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr11:87184192-87185080	IMR90	lung:	n/a	n/a
8	CEBPB	chr11:87174607-87174838	HepG2	liver:	n/a	n/a
9	CTCF	chr11:87174673-87174798	GM10266	blood:	n/a	chr11:87174731-87174747 chr11:87174732-87174753 chr11:87174730-87174748
10	CTCF	chr11:87184260-87184410	HEEpiC	esophagus:	n/a	n/a
11	CTCF	chr11:87238853-87238919	GM10248	blood:	n/a	n/a
12	CTCF	chr11:87174700-87174850	HepG2	liver:	n/a	chr11:87174731-87174747 chr11:87174732-87174753 chr11:87174730-87174748
13	CTCF	chr11:87174680-87174830	SAEC	small airway:	n/a	chr11:87174731-87174747 chr11:87174732-87174753 chr11:87174730-87174748
14	CTCF	chr11:87174620-87174859	GM12878	blood:	n/a	chr11:87174731-87174747 chr11:87174732-87174753 chr11:87174730-87174748
15	CTCF	chr11:87174658-87174811	GM10248	blood:	n/a	chr11:87174731-87174747 chr11:87174732-87174753 chr11:87174730-87174748
16	CTCF	chr11:87212540-87212690	AG09319	gingival:	n/a	n/a
17	CTCF	chr11:87184400-87184550	NHEK	skin:	n/a	n/a
18	CTCF	chr11:87212575-87212647	GM19238	blood:	n/a	n/a
19	CTCF	chr11:87174660-87174810	GM12872	blood:	n/a	chr11:87174731-87174747 chr11:87174732-87174753 chr11:87174730-87174748
20	CTCF	chr11:87174613-87174852	LNCaP	prostate:	n/a	chr11:87174731-87174747 chr11:87174732-87174753 chr11:87174730-87174748
21	CTCF	chr11:87212617-87212651	GM12892	blood:	n/a	n/a
22	CTCF	chr11:87190940-87191090	HepG2	liver:	n/a	n/a
23	CTCF	chr11:87184369-87184489	NHEK	skin:	n/a	n/a
24	CTCF	chr11:87174777-87174799	GM12891	blood:	n/a	n/a
25	CTCF	chr11:87174635-87174848	MCF-7	breast:	n/a	chr11:87174731-87174747 chr11:87174732-87174753 chr11:87174730-87174748
26	CTCF	chr11:87211437-87211459	GM10248	blood:	n/a	n/a
27	CTCF	chr11:87174660-87174810	HBMEC	blood vessel:	n/a	chr11:87174731-87174747 chr11:87174732-87174753 chr11:87174730-87174748
28	CTCF	chr11:87225360-87225510	WERI-Rb-1	eye:	n/a	n/a
29	CTCF	chr11:87212585-87212675	NHEK	skin:	n/a	n/a
30	CTCF	chr11:87212565-87212659	ProgFib	skin:	n/a	n/a
31	CTCF	chr11:87174660-87174810	AG04449	skin:	n/a	chr11:87174731-87174747 chr11:87174732-87174753 chr11:87174730-87174748
32	CTCF	chr11:87174802-87174804	GM12891	blood:	n/a	n/a
33	CTCF	chr11:87212553-87212677	MCF-7	breast:	n/a	n/a
34	CTCF	chr11:87174660-87174810	SAEC	small airway:	n/a	chr11:87174731-87174747 chr11:87174732-87174753 chr11:87174730-87174748
35	CTCF	chr11:87212603-87212669	K562	blood:	n/a	n/a
36	CTCF	chr11:87174630-87174852	K562	blood:	n/a	chr11:87174731-87174747 chr11:87174732-87174753 chr11:87174730-87174748
37	CTCF	chr11:87174622-87174853	Medullo	brain:	n/a	chr11:87174731-87174747 chr11:87174732-87174753 chr11:87174730-87174748
38	CTCF	chr11:87174680-87174830	BJ	skin:	n/a	chr11:87174731-87174747 chr11:87174732-87174753 chr11:87174730-87174748
39	CTCF	chr11:87174611-87174786	A549	lung:	n/a	chr11:87174731-87174747 chr11:87174732-87174753 chr11:87174730-87174748
40	CTCF	chr11:87174660-87174810	HL-60	blood:	n/a	chr11:87174731-87174747 chr11:87174732-87174753 chr11:87174730-87174748
41	CTCF	chr11:87174680-87174830	HAc	cerebellar:	n/a	chr11:87174731-87174747 chr11:87174732-87174753 chr11:87174730-87174748
42	CTCF	chr11:87212528-87212730	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTCF	chr11:87174680-87174830	GM06990	blood:	n/a	chr11:87174731-87174747 chr11:87174732-87174753 chr11:87174730-87174748
44	CTCF	chr11:87174660-87174810	HVMF	connective:	n/a	chr11:87174731-87174747 chr11:87174732-87174753 chr11:87174730-87174748
45	CTCF	chr11:87212520-87212670	HEK293	kidney:	n/a	n/a
46	CTCF	chr11:87174680-87174830	AG04450	lung:	n/a	chr11:87174731-87174747 chr11:87174732-87174753 chr11:87174730-87174748
47	CTCF	chr11:87174600-87174750	GM12865	blood:	n/a	chr11:87174731-87174747 chr11:87174730-87174748
48	CTCF	chr11:87174600-87174750	BJ	skin:	n/a	chr11:87174731-87174747 chr11:87174730-87174748
49	CTCF	chr11:87174660-87174795	SK-N-SH_RA	brain:	n/a	chr11:87174731-87174747 chr11:87174732-87174753 chr11:87174730-87174748
50	CTCF	chr11:87174668-87174837	Pancreas_OC	pancreas:	n/a	chr11:87174731-87174747 chr11:87174732-87174753 chr11:87174730-87174748

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:87224821-87224871	HUVEC	blood vessel:	n/a
2	chr11:87184120-87184170	LNCaP	prostate:	n/a
3	chr11:87184120-87184170	HL-60	blood:	n/a
4	chr11:87204675-87204725	K562	blood:	n/a
5	chr11:87184120-87184170	HEEpiC	esophagus:	n/a
6	chr11:87224821-87224871	Hela-S3	cervix:	n/a
7	chr11:87224821-87224871	GM06990	blood:	n/a
8	chr11:87184120-87184170	ProgFib	skin:	n/a
9	chr11:87184120-87184170	GM19239	blood:	n/a
10	chr11:87204675-87204725	HepG2	liver:	n/a
11	chr11:87204675-87204725	AG10803	skin:	n/a
12	chr11:87184120-87184170	Hepatocyte	liver:	n/a
13	chr11:87224821-87224871	GM12878	blood:	n/a
14	chr11:87224821-87224871	SAEC	small airway:	n/a
15	chr11:87224821-87224871	HEEpiC	esophagus:	n/a
16	chr11:87184120-87184170	Jurkat	blood:	n/a
17	chr11:87204675-87204725	PANC-1	pancreas:	n/a
18	chr11:87224821-87224871	GM19239	blood:	n/a
19	chr11:87184120-87184170	T-47D	breast:	n/a
20	chr11:87184120-87184170	MCF10A-Er-Src	breast:	n/a
21	chr11:87224821-87224871	HCT-116	colon:	n/a
22	chr11:87184120-87184170	HCM	heart:	n/a
23	chr11:87224821-87224871	NHBE	bronchial:	n/a
24	chr11:87224821-87224871	MCF10A-Er-Src	breast:	n/a
25	chr11:87224821-87224871	AoSMC	blood vessel:	n/a
26	chr11:87184120-87184170	SKMC	muscle:	n/a
27	chr11:87204675-87204725	SK-N-MC	brain:	n/a
28	chr11:87224821-87224871	ovcar-3	ovarian:	n/a
29	chr11:87204675-87204725	HL-60	blood:	n/a
30	chr11:87204675-87204725	PFSK-1	brain:	n/a
31	chr11:87184120-87184170	HRE	kidney:	n/a
32	chr11:87204675-87204725	ovcar-3	ovarian:	n/a
33	chr11:87204675-87204725	NHDF-neo	bronchial:	n/a
34	chr11:87224821-87224871	RPTEC	kidney:	n/a
35	chr11:87204675-87204725	H1-hESC	embryonic stem cell:	embryo
36	chr11:87184120-87184170	HRPEpiC	eye:	n/a
37	chr11:87184120-87184170	NH-A	brain:	n/a
38	chr11:87204675-87204725	BE2_C	brain:	n/a
39	chr11:87224821-87224871	AG09309	skin:	n/a
40	chr11:87204675-87204725	HIPEpiC	eye:	n/a
41	chr11:87184120-87184170	HPAEpiC	pulmonary alveolar:	n/a
42	chr11:87184120-87184170	AG10803	skin:	n/a
43	chr11:87204675-87204725	LNCaP	prostate:	n/a
44	chr11:87204675-87204725	AG09319	gingival:	n/a
45	chr11:87224821-87224871	SK-N-SH	brain:	n/a
46	chr11:87184120-87184170	PrEC	prostate:	n/a
47	chr11:87224821-87224871	AG09319	gingival:	n/a
48	chr11:87224821-87224871	SK-N-SH_RA	brain:	n/a
49	chr11:87204675-87204725	SKMC	muscle:	n/a
50	chr11:87224821-87224871	HIPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:87197219..87198779-chr11:87200306..87201927,2	K562	blood:
2	chr11:87174249..87175551-chr11:88277215..88277965,4	K562	blood:
3	chr11:87174299..87174869-chr11:87433363..87434025,2	MCF-7	breast:
4	chr11:87220063..87221996-chr11:87226594..87228726,2	K562	blood:
5	chr11:87162800..87163602-chr11:87174227..87174795,2	K562	blood:
6	chr11:87134513..87137251-chr11:87164100..87165972,2	K562	blood:
7	chr11:87157048..87159158-chr11:87161561..87163817,3	K562	blood:
8	chr11:87162800..87163602-chr11:87174227..87174795,2	K562	blood:
9	chr11:87220063..87221996-chr11:87226594..87228726,2	K562	blood:
10	chr11:87228574..87230526-chr11:87233558..87236260,2	K562	blood:
11	chr11:87241708..87244193-chr11:87247237..87248940,2	K562	blood:
12	chr11:87228574..87230526-chr11:87233558..87236260,2	K562	blood:
13	chr11:87197219..87198779-chr11:87200306..87201927,2	K562	blood:

Variant related genes	Relation type
ENSG00000255391	TF binding region
ENSG00000255391	CpG island

Extended variants
information (count: 2356 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:2356 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs557442382	chr11:87163405-87163406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs553705360	chr11:87163441-87163442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs577382474	chr11:87163465-87163466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs564842990	chr11:87163480-87163481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs60282313	chr11:87163535-87163536	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs573263083	chr11:87163542-87163543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs143059238	chr11:87163615-87163616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs147487732	chr11:87163617-87163618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs562206391	chr11:87163638-87163639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs115122002	chr11:87163682-87163683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs375985625	chr11:87163684-87163685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs368392653	chr11:87163686-87163687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs112960295	chr11:87163690-87163691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs56750299	chr11:87163699-87163700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs201773332	chr11:87163700-87163701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs200569082	chr11:87163701-87163702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs34521519	chr11:87163705-87163706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs79884848	chr11:87163709-87163710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs139857731	chr11:87163722-87163723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs557061615	chr11:87163733-87163734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs138086899	chr11:87163872-87163873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs149517694	chr11:87163892-87163893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs551847687	chr11:87163995-87163996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs73537967	chr11:87164003-87164004	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs376409508	chr11:87164029-87164030	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs11235152	chr11:87164046-87164047	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs79480544	chr11:87164069-87164070	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs79337497	chr11:87164074-87164075	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs529449530	chr11:87164080-87164081	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs537272426	chr11:87164142-87164143	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs73537969	chr11:87164167-87164168	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs559613407	chr11:87164175-87164176	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs74641509	chr11:87164187-87164188	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs191528028	chr11:87164188-87164189	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs148702144	chr11:87164195-87164196	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs373227665	chr11:87164217-87164218	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs376570159	chr11:87164258-87164259	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs556048891	chr11:87164290-87164291	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs539994455	chr11:87164309-87164310	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs575877731	chr11:87164377-87164378	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs562062854	chr11:87164425-87164426	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs529168928	chr11:87164430-87164431	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs146169776	chr11:87164431-87164432	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs183717614	chr11:87164470-87164471	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs533346873	chr11:87164513-87164514	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs76706887	chr11:87164525-87164526	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs371026528	chr11:87164536-87164537	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs188147816	chr11:87164554-87164555	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs144022576	chr11:87164602-87164603	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs528104490	chr11:87164621-87164622	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	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
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Cervical cancer	21062161	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17157792	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	21364760	CNVD
Ovarian neoplasms	16753589	CNVD
Breast cancer	16608533	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Sudden cardiac death	19188705	CNVD
Prostate cancer	16573809	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
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Ductal carcinoma	22052326	CNVD
small cell lung cancer	20016488	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Attention deficit hyperactivity disorder	22241247	CNVD
Breast cancer	21958427	CNVD
Breast cancer	17133270	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Obesity	20622171	CNVD
Renal cell carcinoma	18194544	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:203 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:87151600-87165200	Weak transcription	Colon Smooth Muscle	Colon
2	chr11:87156400-87165000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr11:87156800-87164000	Weak transcription	Fetal Heart	heart
4	chr11:87156800-87164800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr11:87157000-87165000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr11:87157800-87164600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr11:87161800-87163400	Enhancers	HSMM	muscle
8	chr11:87162600-87163400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr11:87162800-87164600	Weak transcription	Fetal Muscle Leg	muscle
10	chr11:87162800-87164800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr11:87162800-87164800	Weak transcription	Fetal Kidney	kidney
12	chr11:87163000-87164400	Weak transcription	HSMMtube	muscle
13	chr11:87163000-87164800	Weak transcription	NHDF-Ad	bronchial
14	chr11:87163000-87165000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr11:87163200-87165000	Weak transcription	Osteobl	bone
16	chr11:87163400-87164600	Weak transcription	HSMM	muscle
17	chr11:87164000-87165400	Enhancers	Psoas Muscle	Psoas
18	chr11:87164000-87165800	Enhancers	Fetal Heart	heart
19	chr11:87164400-87165400	Enhancers	HSMMtube	muscle
20	chr11:87164600-87165400	Enhancers	Fetal Muscle Leg	muscle
21	chr11:87164600-87165400	Enhancers	Skeletal Muscle Female	skeletal muscle
22	chr11:87164600-87165600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr11:87164600-87165800	Enhancers	HSMM	muscle
24	chr11:87164800-87165000	Enhancers	Fetal Kidney	kidney
25	chr11:87164800-87165400	Enhancers	NHDF-Ad	bronchial
26	chr11:87164800-87165600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr11:87164800-87165600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr11:87164800-87165600	Enhancers	Pancreas	Pancrea
29	chr11:87165000-87165200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr11:87165000-87165400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr11:87165000-87165400	Weak transcription	Fetal Kidney	kidney
32	chr11:87165000-87165400	Flanking Active TSS	GM12878-XiMat	blood
33	chr11:87165000-87165600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr11:87165000-87165600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr11:87165000-87165600	Enhancers	Osteobl	bone
36	chr11:87165000-87165800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr11:87165200-87165400	Enhancers	Muscle Satellite Cultured Cells	--
38	chr11:87165200-87165600	Enhancers	Colon Smooth Muscle	Colon
39	chr11:87165400-87165800	Enhancers	Fetal Kidney	kidney
40	chr11:87165400-87166800	Enhancers	GM12878-XiMat	blood
41	chr11:87165600-87167400	Weak transcription	Pancreas	Pancrea
42	chr11:87165800-87173200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr11:87166800-87167200	Weak transcription	GM12878-XiMat	blood
44	chr11:87167200-87167800	Enhancers	GM12878-XiMat	blood
45	chr11:87167800-87170200	Weak transcription	GM12878-XiMat	blood
46	chr11:87170200-87170600	Enhancers	Spleen	Spleen
47	chr11:87170200-87170600	Enhancers	GM12878-XiMat	blood
48	chr11:87173200-87173600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr11:87175600-87176200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr11:87175600-87177800	Enhancers	Fetal Stomach	stomach

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