Variant report

Variant	nsv1049401
Chromosome Location	chr11:105096619-105225032
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	chr11:105168076-105168163	HepG2	liver:	n/a	n/a
2	ATF1	chr11:105140259-105140469	K562	blood:	n/a	n/a
3	BACH1	chr11:105186071-105186351	H1-hESC	embryonic stem cell:	n/a	n/a
4	BRCA1	chr11:105115074-105115781	Hela-S3	cervix:	n/a	chr11:105115556-105115563
5	BRCA1	chr11:105189118-105189153	GM12878	blood:	n/a	n/a
6	CEBPB	chr11:105197977-105198224	HepG2	liver:	n/a	chr11:105198065-105198076
7	CEBPB	chr11:105100073-105100378	HepG2	liver:	n/a	chr11:105100246-105100255 chr11:105100244-105100257 chr11:105100244-105100257 chr11:105100246-105100255 chr11:105100246-105100255
8	CEBPB	chr11:105172168-105172394	HepG2	liver:	n/a	chr11:105172303-105172314
9	CEBPB	chr11:105100027-105100610	Hela-S3	cervix:	n/a	chr11:105100246-105100255 chr11:105100244-105100257 chr11:105100244-105100257 chr11:105100246-105100255 chr11:105100246-105100255
10	CEBPB	chr11:105097012-105097281	HepG2	liver:	n/a	chr11:105097173-105097186 chr11:105097174-105097185
11	CEBPB	chr11:105136545-105136918	Hela-S3	cervix:	n/a	chr11:105136722-105136739
12	CEBPB	chr11:105224992-105225215	HepG2	liver:	n/a	n/a
13	CEBPB	chr11:105099967-105100442	IMR90	lung:	n/a	chr11:105100246-105100255 chr11:105100244-105100257 chr11:105100244-105100257 chr11:105100246-105100255 chr11:105100246-105100255
14	CEBPB	chr11:105100132-105100371	A549	lung:	n/a	chr11:105100246-105100255 chr11:105100244-105100257 chr11:105100244-105100257 chr11:105100246-105100255 chr11:105100246-105100255
15	CEBPB	chr11:105113646-105113946	IMR90	lung:	n/a	chr11:105113793-105113802 chr11:105113793-105113802
16	CEBPB	chr11:105101335-105101671	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr11:105207539-105207596	HepG2	liver:	n/a	chr11:105207568-105207579
18	CEBPB	chr11:105100148-105100348	H1-hESC	embryonic stem cell:	n/a	chr11:105100246-105100255 chr11:105100244-105100257 chr11:105100244-105100257 chr11:105100246-105100255 chr11:105100246-105100255
19	CEBPB	chr11:105117710-105118084	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr11:105115154-105115582	IMR90	lung:	n/a	n/a
21	CEBPB	chr11:105136627-105136884	IMR90	lung:	n/a	chr11:105136722-105136739
22	CEBPB	chr11:105115181-105115443	A549	lung:	n/a	n/a
23	CEBPB	chr11:105191426-105191626	HepG2	liver:	n/a	n/a
24	CEBPB	chr11:105225005-105225176	A549	lung:	n/a	n/a
25	CEBPB	chr11:105197911-105198192	IMR90	lung:	n/a	chr11:105198065-105198076
26	CEBPB	chr11:105097017-105097802	Hela-S3	cervix:	n/a	chr11:105097173-105097186 chr11:105097174-105097185
27	CEBPB	chr11:105097001-105097342	IMR90	lung:	n/a	chr11:105097173-105097186 chr11:105097174-105097185
28	CEBPB	chr11:105114894-105115596	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr11:105172157-105172482	IMR90	lung:	n/a	chr11:105172303-105172314
30	CHD2	chr11:105115153-105115538	Hela-S3	cervix:	n/a	n/a
31	CTCF	chr11:105186160-105186310	GM12872	blood:	n/a	n/a
32	CTCF	chr11:105186120-105186270	HCM	heart:	n/a	n/a
33	CTCF	chr11:105186140-105186290	HEEpiC	esophagus:	n/a	n/a
34	CTCF	chr11:105186200-105186350	HMF	breast:	n/a	n/a
35	CTCF	chr11:105186170-105186294	HUVEC	blood vessel:	n/a	n/a
36	CTCF	chr11:105186031-105186376	HepG2	liver:	n/a	n/a
37	CTCF	chr11:105098280-105098430	HCPEpiC	choroid plexus:	n/a	n/a
38	CTCF	chr11:105186089-105186459	HCT-116	colon:	n/a	n/a
39	CTCF	chr11:105186160-105186310	RPTEC	kidney:	n/a	n/a
40	CTCF	chr11:105194994-105195039	LNCaP	prostate:	n/a	n/a
41	CTCF	chr11:105186140-105186290	WERI-Rb-1	eye:	n/a	n/a
42	CTCF	chr11:105186140-105186290	Caco-2	colon:	n/a	n/a
43	CTCF	chr11:105186160-105186310	HepG2	liver:	n/a	n/a
44	CTCF	chr11:105186120-105186270	Caco-2	colon:	n/a	n/a
45	CTCF	chr11:105186080-105186230	HFF-Myc	foreskin:	n/a	n/a
46	CTCF	chr11:105186160-105186310	SAEC	small airway:	n/a	n/a
47	CTCF	chr11:105186140-105186290	SAEC	small airway:	n/a	n/a
48	CTCF	chr11:105186140-105186296	HepG2	liver:	n/a	n/a
49	CTCF	chr11:105186120-105186270	BE2_C	brain:	n/a	n/a
50	CTCF	chr11:105186039-105186314	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:105096701-105096751	HCF	heart:	n/a
2	chr11:105096701-105096751	HCF	heart:	n/a
3	chr11:105096701-105096751	IMR90	lung:	fetal
4	chr11:105096701-105096751	GM12891	blood:	n/a
5	chr11:105096701-105096751	ovcar-3	ovarian:	n/a
6	chr11:105096701-105096751	T-47D	breast:	n/a
7	chr11:105169034-105169084	HRE	kidney:	n/a
8	chr11:105169034-105169084	PFSK-1	brain:	n/a
9	chr11:105096701-105096751	LNCaP	prostate:	n/a
10	chr11:105169034-105169084	SKMC	muscle:	n/a
11	chr11:105169034-105169084	AG09319	gingival:	n/a
12	chr11:105096701-105096751	HAEpiC	amniotic membrane:	n/a
13	chr11:105169034-105169084	ovcar-3	ovarian:	n/a
14	chr11:105096701-105096751	AG09309	skin:	n/a
15	chr11:105096701-105096751	NB4	blood:	n/a
16	chr11:105096701-105096751	HRCEpiC	kidney:	n/a
17	chr11:105096701-105096751	MCF10A-Er-Src	breast:	n/a
18	chr11:105096701-105096751	HepG2	liver:	n/a
19	chr11:105096701-105096751	HNPCEpiC	eye:	n/a
20	chr11:105096701-105096751	Jurkat	blood:	n/a
21	chr11:105096701-105096751	HCT-116	colon:	n/a
22	chr11:105096701-105096751	HL-60	blood:	n/a
23	chr11:105169034-105169084	SAEC	small airway:	n/a
24	chr11:105169034-105169084	NT2-D1	testis:	n/a
25	chr11:105096701-105096751	HRE	kidney:	n/a
26	chr11:105096701-105096751	AoSMC	blood vessel:	n/a
27	chr11:105169034-105169084	U87	brain:	n/a
28	chr11:105169034-105169084	Caco-2	colon:	n/a
29	chr11:105169034-105169084	HUVEC	blood vessel:	n/a
30	chr11:105169034-105169084	SK-N-MC	brain:	n/a
31	chr11:105096701-105096751	NHDF-neo	bronchial:	n/a
32	chr11:105169034-105169084	GM12878	blood:	n/a
33	chr11:105096701-105096751	RPTEC	kidney:	n/a
34	chr11:105096701-105096751	PANC-1	pancreas:	n/a
35	chr11:105169034-105169084	HepG2	liver:	n/a
36	chr11:105169034-105169084	GM19239	blood:	n/a
37	chr11:105169034-105169084	HEEpiC	esophagus:	n/a
38	chr11:105169034-105169084	AG04450	lung:	fetal
39	chr11:105169034-105169084	GM12892	blood:	n/a
40	chr11:105096701-105096751	HEEpiC	esophagus:	n/a
41	chr11:105169034-105169084	NHBE	bronchial:	n/a
42	chr11:105096701-105096751	GM06990	blood:	n/a
43	chr11:105169034-105169084	AG04449	skin:	fetal
44	chr11:105096701-105096751	HIPEpiC	eye:	n/a
45	chr11:105096701-105096751	SKMC	muscle:	n/a
46	chr11:105096701-105096751	GM19239	blood:	n/a
47	chr11:105096701-105096751	HEK293	kidney:	embryo
48	chr11:105096701-105096751	MCF-7	breast:	n/a
49	chr11:105169034-105169084	HIPEpiC	eye:	n/a
50	chr11:105096701-105096751	Caco-2	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:105182301..105184652-chr11:105187626..105190416,2	K562	blood:
2	chr11:105153100..105154691-chr11:105182202..105183896,2	MCF-7	breast:
3	chr11:105153100..105154691-chr11:105182202..105183896,2	MCF-7	breast:
4	chr11:105182301..105184652-chr11:105187626..105190416,2	K562	blood:
5	chr11:105114147..105114647-chr9:140135285..140136197,2	Hela-S3	cervix:
6	chr11:105000203..105002774-chr11:105190534..105192628,2	K562	blood:
7	chr11:105125650..105127473-chr11:105130695..105132691,2	K562	blood:
8	chr11:105125650..105127473-chr11:105130695..105132691,2	K562	blood:
9	chr11:105173283..105175054-chr11:105186519..105189331,2	K562	blood:
10	chr11:105173283..105175054-chr11:105186519..105189331,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CARD18-2	chr11:105130369-105130412	ENSG00000254998.1
2	lnc-CARD18-2	chr11:105138990-105139038	ENSG00000254998.1

Variant related genes	Relation type
ENSG00000255336	TF binding region
ENSG00000255336	CpG island
ENSG00000188229	chromatin interactions

Extended variants
information (count: 1918 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:1918 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs534231037	chr11:105096633-105096634	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs555680421	chr11:105096647-105096648	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs371316234	chr11:105096680-105096681	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs559129437	chr11:105096702-105096703	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs184531697	chr11:105096781-105096782	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs112210184	chr11:105096791-105096792	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs563201720	chr11:105096793-105096794	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs575318910	chr11:105096794-105096795	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs145931861	chr11:105096946-105096947	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs11226667	chr11:105096976-105096977	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs190047190	chr11:105097026-105097027	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs139973113	chr11:105097076-105097077	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs193051101	chr11:105097089-105097090	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs148191867	chr11:105097090-105097091	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs367794579	chr11:105097097-105097098	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs17104013	chr11:105097112-105097113	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs569227319	chr11:105097147-105097148	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs185082997	chr11:105097189-105097190	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs6591117	chr11:105097200-105097201	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs551645794	chr11:105097255-105097256	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs541558386	chr11:105097269-105097270	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs534171092	chr11:105097303-105097304	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs112932321	chr11:105097314-105097315	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs555619162	chr11:105097318-105097319	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs371666876	chr11:105097319-105097320	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs554815160	chr11:105097325-105097326	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs567655314	chr11:105097326-105097327	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs74526116	chr11:105097353-105097354	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs556917784	chr11:105097451-105097452	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs7947531	chr11:105097465-105097466	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs144568325	chr11:105097541-105097542	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs557614791	chr11:105097599-105097600	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs368033561	chr11:105097601-105097602	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs540466291	chr11:105097623-105097624	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs78881570	chr11:105097624-105097625	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs189979678	chr11:105097680-105097681	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs142885515	chr11:105097711-105097712	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs562911683	chr11:105097784-105097785	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs375134208	chr11:105097839-105097840	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs12281652	chr11:105097845-105097846	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs551852302	chr11:105097874-105097875	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs566654992	chr11:105097909-105097910	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs111951823	chr11:105097933-105097934	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs181216396	chr11:105097939-105097940	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs151058819	chr11:105097940-105097941	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs538537733	chr11:105097983-105097984	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs556622411	chr11:105097988-105097989	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs375531528	chr11:105098058-105098059	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs185488322	chr11:105098087-105098088	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs1449045	chr11:105098107-105098108	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:96)

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
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
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
Melanoma	17363583	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
Obesity	19966786	CNVD
Prostate cancer	18632612	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	17142309	CNVD

Chromatin state (count:191 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:105092600-105097800	Weak transcription	Primary neutrophils fromperipheralblood	blood
2	chr11:105095400-105097600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr11:105095400-105101600	Weak transcription	Psoas Muscle	Psoas
4	chr11:105096000-105101400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr11:105096200-105100600	Weak transcription	NHEK	skin
6	chr11:105096400-105098200	Enhancers	Fetal Lung	lung
7	chr11:105096800-105098000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr11:105097000-105102200	Enhancers	Hela-S3	cervix
9	chr11:105097200-105098400	Enhancers	HepG2	liver
10	chr11:105097600-105098200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr11:105097600-105098400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr11:105097600-105098400	Enhancers	Fetal Intestine Large	intestine
13	chr11:105097600-105098400	Enhancers	Fetal Intestine Small	intestine
14	chr11:105097800-105098600	Enhancers	Primary neutrophils fromperipheralblood	blood
15	chr11:105098000-105098600	Enhancers	Primary monocytes fromperipheralblood	blood
16	chr11:105098000-105099600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr11:105098400-105098600	Enhancers	HUVEC	blood vessel
18	chr11:105098400-105099800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr11:105098600-105100400	Weak transcription	Primary monocytes fromperipheralblood	blood
20	chr11:105098800-105102800	Weak transcription	HUVEC	blood vessel
21	chr11:105099400-105099600	Enhancers	Sigmoid Colon	Sigmoid Colon
22	chr11:105099400-105100400	Enhancers	NHDF-Ad	bronchial
23	chr11:105099400-105100800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr11:105099400-105100800	Enhancers	NHLF	lung
25	chr11:105099600-105100600	Enhancers	Adipose Nuclei	Adipose
26	chr11:105099600-105100800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr11:105099600-105100800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr11:105099600-105100800	Enhancers	Osteobl	bone
29	chr11:105099800-105100800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr11:105099800-105100800	Enhancers	Muscle Satellite Cultured Cells	--
31	chr11:105100000-105101200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr11:105100400-105100600	Flanking Active TSS	NHDF-Ad	bronchial
33	chr11:105100400-105100800	Enhancers	Primary monocytes fromperipheralblood	blood
34	chr11:105100400-105100800	Enhancers	Placenta	Placenta
35	chr11:105100400-105101600	Enhancers	Skeletal Muscle Female	skeletal muscle
36	chr11:105100400-105102400	Enhancers	Rectal Mucosa Donor 31	rectum
37	chr11:105100600-105100800	Enhancers	NHEK	skin
38	chr11:105100600-105101600	Enhancers	NHDF-Ad	bronchial
39	chr11:105100800-105101200	Weak transcription	NHEK	skin
40	chr11:105100800-105104600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr11:105101200-105101600	Enhancers	NHEK	skin
42	chr11:105101400-105101800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr11:105102800-105104000	Enhancers	HUVEC	blood vessel
44	chr11:105103200-105103600	Enhancers	Dnd41	blood
45	chr11:105104000-105114400	Weak transcription	HUVEC	blood vessel
46	chr11:105104600-105104800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr11:105105000-105105200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr11:105105400-105106600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr11:105106600-105108200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr11:105107200-105107800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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