Variant report

Variant	nsv1037454
Chromosome Location	chr11:102487521-102601233
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	ARID3A	chr11:102511651-102511855	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:102495580-102495752	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:102495975-102496301	HepG2	liver:	n/a	n/a
4	ARID3A	chr11:102537194-102537364	HepG2	liver:	n/a	n/a
5	ATF1	chr11:102491874-102492087	K562	blood:	n/a	n/a
6	ATF1	chr11:102487671-102487795	K562	blood:	n/a	n/a
7	ATF3	chr11:102524611-102524876	K562	blood:	n/a	n/a
8	BACH1	chr11:102492007-102492066	K562	blood:	n/a	n/a
9	BATF	chr11:102492033-102492305	GM12878	blood:	n/a	n/a
10	BATF	chr11:102492069-102492276	GM12878	blood:	n/a	n/a
11	BCL3	chr11:102524341-102525162	GM12878	blood:	n/a	n/a
12	BCL3	chr11:102524310-102525220	GM12878	blood:	n/a	chr11:102524339-102524348
13	BHLHE40	chr11:102495909-102496304	HepG2	liver:	n/a	n/a
14	BHLHE40	chr11:102524704-102524992	A549	lung:	n/a	chr11:102524722-102524743 chr11:102524727-102524736 chr11:102524728-102524737 chr11:102524726-102524739 chr11:102524728-102524737 chr11:102524729-102524738
15	BHLHE40	chr11:102524627-102525032	GM12878	blood:	n/a	chr11:102524722-102524743 chr11:102524727-102524736 chr11:102524728-102524737 chr11:102524726-102524739 chr11:102524728-102524737 chr11:102524729-102524738
16	BHLHE40	chr11:102492978-102493475	HepG2	liver:	n/a	n/a
17	BHLHE40	chr11:102493095-102493377	K562	blood:	n/a	n/a
18	BHLHE40	chr11:102524470-102525126	K562	blood:	n/a	chr11:102524722-102524743 chr11:102524727-102524736 chr11:102524728-102524737 chr11:102524726-102524739 chr11:102524728-102524737 chr11:102524729-102524738
19	BHLHE40	chr11:102537187-102537332	K562	blood:	n/a	n/a
20	BHLHE40	chr11:102524541-102525081	HepG2	liver:	n/a	chr11:102524722-102524743 chr11:102524727-102524736 chr11:102524728-102524737 chr11:102524726-102524739 chr11:102524728-102524737 chr11:102524729-102524738
21	BHLHE40	chr11:102501366-102501525	HepG2	liver:	n/a	n/a
22	BHLHE40	chr11:102493052-102493358	HepG2	liver:	n/a	n/a
23	BRCA1	chr11:102537167-102537323	Hela-S3	cervix:	n/a	n/a
24	CBX3	chr11:102524402-102525097	K562	blood:	n/a	n/a
25	CBX3	chr11:102491784-102492229	K562	blood:	n/a	n/a
26	CEBPB	chr11:102592260-102592648	IMR90	lung:	n/a	chr11:102592407-102592418
27	CEBPB	chr11:102592316-102592617	A549	lung:	n/a	chr11:102592407-102592418
28	CEBPB	chr11:102508428-102508888	A549	lung:	n/a	chr11:102508650-102508661
29	CEBPB	chr11:102504596-102504903	A549	lung:	n/a	n/a
30	CEBPB	chr11:102588054-102588342	K562	blood:	n/a	chr11:102588212-102588223
31	CEBPB	chr11:102508478-102508833	H1-hESC	embryonic stem cell:	n/a	chr11:102508650-102508661
32	CEBPB	chr11:102508469-102508810	MCF-7	breast:	n/a	chr11:102508650-102508661
33	CEBPB	chr11:102592238-102592596	HepG2	liver:	n/a	chr11:102592407-102592418
34	CEBPB	chr11:102590097-102590204	HepG2	liver:	n/a	chr11:102590174-102590185
35	CEBPB	chr11:102513601-102513647	HepG2	liver:	n/a	n/a
36	CEBPB	chr11:102511621-102511979	HepG2	liver:	n/a	n/a
37	CEBPB	chr11:102508550-102508750	Hela-S3	cervix:	n/a	chr11:102508650-102508661
38	CEBPB	chr11:102580024-102580151	HepG2	liver:	n/a	chr11:102580095-102580106
39	CEBPB	chr11:102588090-102588379	IMR90	lung:	n/a	chr11:102588212-102588223
40	CEBPB	chr11:102588116-102588382	A549	lung:	n/a	chr11:102588212-102588223
41	CEBPB	chr11:102504649-102504881	IMR90	lung:	n/a	n/a
42	CEBPB	chr11:102592353-102592461	Hela-S3	cervix:	n/a	chr11:102592407-102592418
43	CEBPB	chr11:102588167-102588261	Hela-S3	cervix:	n/a	chr11:102588212-102588223
44	CEBPB	chr11:102579935-102580268	IMR90	lung:	n/a	chr11:102580095-102580106
45	CEBPB	chr11:102508350-102508988	HCT-116	colon:	n/a	chr11:102508650-102508661
46	CEBPB	chr11:102579995-102580195	H1-hESC	embryonic stem cell:	n/a	chr11:102580095-102580106
47	CEBPB	chr11:102551914-102551941	IMR90	lung:	n/a	n/a
48	CEBPB	chr11:102508480-102508834	A549	lung:	n/a	chr11:102508650-102508661
49	CEBPB	chr11:102504632-102504870	HepG2	liver:	n/a	n/a
50	CEBPB	chr11:102598504-102598971	IMR90	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:102583226-102583276	K562	blood:	n/a
2	chr11:102583226-102583276	K562	blood:	n/a
3	chr11:102496115-102496165	BE2_C	brain:	n/a
4	chr11:102576374-102576424	HRE	kidney:	n/a
5	chr11:102595300-102595350	CMK	blood:	n/a
6	chr11:102583226-102583276	HMEC	breast:	n/a
7	chr11:102496501-102496551	AG09309	skin:	n/a
8	chr11:102576508-102576558	GM12878	blood:	n/a
9	chr11:102595300-102595350	HPAEpiC	pulmonary alveolar:	n/a
10	chr11:102576469-102576519	MCF10A-Er-Src	breast:	n/a
11	chr11:102576374-102576424	ProgFib	skin:	n/a
12	chr11:102496159-102496209	HMEC	breast:	n/a
13	chr11:102496115-102496165	A549	lung:	n/a
14	chr11:102496159-102496209	NT2-D1	testis:	n/a
15	chr11:102496501-102496551	H1-hESC	embryonic stem cell:	embryo
16	chr11:102496501-102496551	ECC-1	luminal epithelium:	n/a
17	chr11:102496115-102496165	GM12891	blood:	n/a
18	chr11:102556583-102556633	NHBE	bronchial:	n/a
19	chr11:102583226-102583276	NB4	blood:	n/a
20	chr11:102576094-102576144	Caco-2	colon:	n/a
21	chr11:102496159-102496209	K562	blood:	n/a
22	chr11:102496104-102496154	CMK	blood:	n/a
23	chr11:102576469-102576519	T-47D	breast:	n/a
24	chr11:102576469-102576519	Hela-S3	cervix:	n/a
25	chr11:102496159-102496209	PrEC	prostate:	n/a
26	chr11:102496115-102496165	HMEC	breast:	n/a
27	chr11:102576094-102576144	HNPCEpiC	eye:	n/a
28	chr11:102583226-102583276	HNPCEpiC	eye:	n/a
29	chr11:102600758-102600808	HL-60	blood:	n/a
30	chr11:102496104-102496154	ProgFib	skin:	n/a
31	chr11:102600758-102600808	GM12892	blood:	n/a
32	chr11:102576094-102576144	HL-60	blood:	n/a
33	chr11:102583226-102583276	HepG2	liver:	n/a
34	chr11:102600758-102600808	NHDF-neo	bronchial:	n/a
35	chr11:102576094-102576144	HEK293	kidney:	embryo
36	chr11:102496159-102496209	U87	brain:	n/a
37	chr11:102496115-102496165	HPAEpiC	pulmonary alveolar:	n/a
38	chr11:102583226-102583276	NT2-D1	testis:	n/a
39	chr11:102576508-102576558	SKMC	muscle:	n/a
40	chr11:102496104-102496154	SKMC	muscle:	n/a
41	chr11:102496115-102496165	AG10803	skin:	n/a
42	chr11:102496115-102496165	Jurkat	blood:	n/a
43	chr11:102576469-102576519	PFSK-1	brain:	n/a
44	chr11:102496115-102496165	MCF10A-Er-Src	breast:	n/a
45	chr11:102496501-102496551	ProgFib	skin:	n/a
46	chr11:102496104-102496154	HMEC	breast:	n/a
47	chr11:102576094-102576144	HCM	heart:	n/a
48	chr11:102576508-102576558	HUVEC	blood vessel:	n/a
49	chr11:102576094-102576144	LNCaP	prostate:	n/a
50	chr11:102577488-102577538	Hela-S3	cervix:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:102587738..102589821-chr11:102592167..102593864,2	K562	blood:
2	chr11:102591508..102593641-chr11:102596707..102599054,3	K562	blood:
3	chr11:102391762..102394705-chr11:102534694..102536985,2	K562	blood:
4	chr11:102587738..102589821-chr11:102592167..102593864,2	K562	blood:
5	chr11:102485385..102487905-chr11:102489237..102492124,3	K562	blood:
6	chr11:102482496..102484239-chr11:102491077..102493639,2	K562	blood:
7	chr11:102404921..102405719-chr11:102536805..102537368,2	MCF-7	breast:
8	chr11:102485385..102487905-chr11:102489237..102492124,3	K562	blood:
9	chr11:102463844..102464395-chr11:102537160..102537675,2	MCF-7	breast:
10	chr11:102485326..102485970-chr11:102537194..102537739,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-817J15.3.1-2	chr11:102497390-102497511	ENSG00000256916.1
2	lnc-RP11-817J15.3.1-1	chr11:102511885-102512066	XLOC_009261
3	lnc-RP11-817J15.3.1-1	chr11:102548434-102548515	XLOC_009261
4	lnc-RP11-817J15.3.1-2	chr11:102497870-102498042	ENSG00000256916.1
5	lnc-RP11-817J15.3.1-1	chr11:102551985-102552089	XLOC_009261
6	lnc-RP11-817J15.3.1-1	chr11:102548434-102548516	XLOC_009261
7	lnc-RP11-817J15.3.1-1	chr11:102511869-102512066	XLOC_009261
8	lnc-RP11-817J15.3.1-2	chr11:102498440-102498801	ENSG00000256916.1

Variant related genes	Relation type
ENSG00000255798	TF binding region
MMP20	TF binding region
MMP27	TF binding region
MMP8	TF binding region
ENSG00000255798	CpG island
MMP20	CpG island
MMP27	CpG island
MMP8	CpG island
ENSG00000118113	chromatin interactions

Extended variants
information (count: 4985 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:4985 , 50 per page) page: 1 2 3 4 5 6 7 ... 100

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs370896953	chr11:102487532-102487533	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs143362660	chr11:102487545-102487546	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs374230120	chr11:102487574-102487575	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs376926048	chr11:102487585-102487586	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs146053692	chr11:102487591-102487592	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs559904677	chr11:102487593-102487594	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs532136091	chr11:102487605-102487606	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs371625120	chr11:102487620-102487621	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs373684205	chr11:102487621-102487622	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs367552668	chr11:102487628-102487629	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs552450761	chr11:102487629-102487630	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs61730848	chr11:102487643-102487644	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs200482846	chr11:102487663-102487664	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs199926748	chr11:102487664-102487665	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs373917419	chr11:102487665-102487666	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs143113210	chr11:102487678-102487679	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs185057360	chr11:102487686-102487687	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs140041158	chr11:102487707-102487708	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs368095511	chr11:102487714-102487715	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs138308694	chr11:102487715-102487716	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs553644151	chr11:102487745-102487746	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs371858298	chr11:102487747-102487748	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs202146356	chr11:102487753-102487754	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs376574181	chr11:102487754-102487755	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs539985502	chr11:102487779-102487780	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs370844687	chr11:102487782-102487783	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs368618439	chr11:102487797-102487798	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs375856007	chr11:102487804-102487805	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs17099087	chr11:102487813-102487814	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs150897495	chr11:102487814-102487815	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs201263606	chr11:102487815-102487816	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs113993931	chr11:102487821-102487822	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs544220123	chr11:102487825-102487826	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs76853724	chr11:102487844-102487845	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs574232384	chr11:102487850-102487851	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs546607391	chr11:102487883-102487884	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs560111819	chr11:102487921-102487922	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs569843968	chr11:102487927-102487928	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs17099090	chr11:102487932-102487933	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs552054791	chr11:102487970-102487971	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs190300938	chr11:102487994-102487995	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs531485085	chr11:102488038-102488039	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs551001461	chr11:102488052-102488053	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs150025273	chr11:102488053-102488054	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs536601570	chr11:102488070-102488071	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs17099093	chr11:102488072-102488073	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs1317947	chr11:102488073-102488074	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs145375415	chr11:102488074-102488075	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs376331804	chr11:102488107-102488108	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs2280211	chr11:102488131-102488132	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:92)

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
Melanoma	22183965	CNVD
Breast cancer	21958427	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Renal cell carcinoma	18194544	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
low-grade B-cell lymphoma tumor	18367492	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Mental retardation	19966786	CNVD
Non-small cell lung cancer	21829676	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Multiple myeloma	16616336	CNVD
Intracranial aneurysm	16715129	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16912164	CNVD
Ovarian cancer	21720365	CNVD
Melanoma	17363583	CNVD
Chronic lymphocytic leukemia	17805327	CNVD
Glioblastoma multiforme	22286061	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Neuroblastoma	17327916	CNVD
Melanoma	20877625	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:398 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:102484200-102488600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr11:102484200-102491200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr11:102484400-102488400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr11:102485600-102490800	Weak transcription	Fetal Intestine Large	intestine
5	chr11:102485600-102492800	Weak transcription	Fetal Intestine Small	intestine
6	chr11:102486200-102487800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr11:102486200-102488600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr11:102486400-102488200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr11:102486400-102488400	Weak transcription	HUES64 Cell Line	embryonic stem cell
10	chr11:102486400-102488600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr11:102486600-102488200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr11:102486600-102488200	Weak transcription	H1 Cell Line	embryonic stem cell
13	chr11:102486600-102491600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr11:102486800-102487800	Enhancers	HepG2	liver
15	chr11:102486800-102488200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr11:102486800-102488200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
17	chr11:102487000-102488600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr11:102487000-102489200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr11:102487000-102491200	Weak transcription	HUVEC	blood vessel
20	chr11:102487000-102494800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr11:102487000-102497000	Weak transcription	HSMMtube	muscle
22	chr11:102487200-102491400	Weak transcription	A549	lung
23	chr11:102487800-102491600	Weak transcription	HepG2	liver
24	chr11:102488200-102488400	Enhancers	H1 Cell Line	embryonic stem cell
25	chr11:102488200-102488600	Enhancers	ES-I3 Cell Line	embryonic stem cell
26	chr11:102488200-102488600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr11:102488200-102488600	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr11:102488200-102488800	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr11:102488200-102488800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr11:102488400-102488600	Enhancers	HUES64 Cell Line	embryonic stem cell
31	chr11:102488400-102488800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr11:102488400-102488800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr11:102488600-102488800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr11:102488800-102491800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr11:102489600-102489800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr11:102490800-102491200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr11:102490800-102491600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr11:102490800-102491600	Enhancers	Fetal Intestine Large	intestine
39	chr11:102491200-102492000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr11:102491200-102492600	Enhancers	K562	blood
41	chr11:102491200-102493600	Enhancers	HUVEC	blood vessel
42	chr11:102491400-102492000	Enhancers	NHLF	lung
43	chr11:102491400-102492200	Enhancers	Osteobl	bone
44	chr11:102491400-102492400	Enhancers	Muscle Satellite Cultured Cells	--
45	chr11:102491400-102492400	Enhancers	A549	lung
46	chr11:102491400-102492400	Enhancers	GM12878-XiMat	blood
47	chr11:102491600-102491800	Enhancers	Aorta	Aorta
48	chr11:102491600-102492000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr11:102491600-102492200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr11:102491600-102493000	Weak transcription	Fetal Intestine Large	intestine

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