Variant report

Variant	nsv1045900
Chromosome Location	chr11:105015999-105138877
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	chr11:105050156-105050694	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:105070882-105071074	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:105056096-105056101	K562	blood:	n/a	n/a
4	ARID3A	chr11:105073148-105074832	HepG2	liver:	n/a	chr11:105073641-105073657
5	BHLHE40	chr11:105073400-105073945	HepG2	liver:	n/a	n/a
6	BRCA1	chr11:105082656-105083279	Hela-S3	cervix:	n/a	n/a
7	BRCA1	chr11:105115074-105115781	Hela-S3	cervix:	n/a	chr11:105115556-105115563
8	CBX3	chr11:105073626-105073980	HCT-116	colon:	n/a	n/a
9	CEBPB	chr11:105060329-105060710	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr11:105097001-105097342	IMR90	lung:	n/a	chr11:105097173-105097186 chr11:105097174-105097185
11	CEBPB	chr11:105060352-105060716	HepG2	liver:	n/a	n/a
12	CEBPB	chr11:105100027-105100610	Hela-S3	cervix:	n/a	chr11:105100246-105100255 chr11:105100244-105100257 chr11:105100244-105100257 chr11:105100246-105100255 chr11:105100246-105100255
13	CEBPB	chr11:105136545-105136918	Hela-S3	cervix:	n/a	chr11:105136722-105136739
14	CEBPB	chr11:105037990-105038319	Hela-S3	cervix:	n/a	chr11:105038152-105038161 chr11:105038150-105038163 chr11:105038150-105038161 chr11:105038152-105038161 chr11:105038150-105038163 chr11:105038152-105038161
15	CEBPB	chr11:105029570-105029888	HepG2	liver:	n/a	chr11:105029701-105029712
16	CEBPB	chr11:105067093-105067309	A549	lung:	n/a	n/a
17	CEBPB	chr11:105051822-105052631	IMR90	lung:	n/a	n/a
18	CEBPB	chr11:105021083-105021294	HepG2	liver:	n/a	chr11:105021130-105021141
19	CEBPB	chr11:105060341-105060715	IMR90	lung:	n/a	n/a
20	CEBPB	chr11:105026867-105027253	Hela-S3	cervix:	n/a	chr11:105027229-105027240
21	CEBPB	chr11:105136627-105136884	IMR90	lung:	n/a	chr11:105136722-105136739
22	CEBPB	chr11:105113646-105113946	IMR90	lung:	n/a	chr11:105113793-105113802 chr11:105113793-105113802
23	CEBPB	chr11:105026850-105027169	HepG2	liver:	n/a	n/a
24	CEBPB	chr11:105067024-105067373	IMR90	lung:	n/a	n/a
25	CEBPB	chr11:105117710-105118084	Hela-S3	cervix:	n/a	n/a
26	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
27	CEBPB	chr11:105037987-105038303	H1-hESC	embryonic stem cell:	n/a	chr11:105038152-105038161 chr11:105038150-105038163 chr11:105038150-105038161 chr11:105038152-105038161 chr11:105038150-105038163 chr11:105038152-105038161
28	CEBPB	chr11:105097017-105097802	Hela-S3	cervix:	n/a	chr11:105097173-105097186 chr11:105097174-105097185
29	CEBPB	chr11:105101335-105101671	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr11:105060375-105060703	A549	lung:	n/a	n/a
31	CEBPB	chr11:105022378-105023742	Hela-S3	cervix:	n/a	chr11:105023107-105023118 chr11:105023123-105023134
32	CEBPB	chr11:105037971-105038347	IMR90	lung:	n/a	chr11:105038152-105038161 chr11:105038150-105038163 chr11:105038150-105038161 chr11:105038152-105038161 chr11:105038150-105038163 chr11:105038152-105038161
33	CEBPB	chr11:105029635-105029866	IMR90	lung:	n/a	chr11:105029701-105029712
34	CEBPB	chr11:105097012-105097281	HepG2	liver:	n/a	chr11:105097173-105097186 chr11:105097174-105097185
35	CEBPB	chr11:105037965-105038340	K562	blood:	n/a	chr11:105038152-105038161 chr11:105038150-105038163 chr11:105038150-105038161 chr11:105038152-105038161 chr11:105038150-105038163 chr11:105038152-105038161
36	CEBPB	chr11:105038034-105038344	A549	lung:	n/a	chr11:105038152-105038161 chr11:105038150-105038163 chr11:105038150-105038161 chr11:105038152-105038161 chr11:105038150-105038163 chr11:105038152-105038161
37	CEBPB	chr11:105100073-105100378	HepG2	liver:	n/a	chr11:105100246-105100255 chr11:105100244-105100257 chr11:105100244-105100257 chr11:105100246-105100255 chr11:105100246-105100255
38	CEBPB	chr11:105067033-105067343	HepG2	liver:	n/a	n/a
39	CEBPB	chr11:105100132-105100371	A549	lung:	n/a	chr11:105100246-105100255 chr11:105100244-105100257 chr11:105100244-105100257 chr11:105100246-105100255 chr11:105100246-105100255
40	CEBPB	chr11:105115181-105115443	A549	lung:	n/a	n/a
41	CEBPB	chr11:105095255-105095538	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr11:105050365-105050599	HepG2	liver:	n/a	chr11:105050529-105050542
43	CEBPB	chr11:105022487-105023313	IMR90	lung:	n/a	chr11:105023107-105023118 chr11:105023123-105023134
44	CEBPB	chr11:105037981-105038342	HepG2	liver:	n/a	chr11:105038152-105038161 chr11:105038150-105038163 chr11:105038150-105038161 chr11:105038152-105038161 chr11:105038150-105038163 chr11:105038152-105038161
45	CEBPB	chr11:105099967-105100442	IMR90	lung:	n/a	chr11:105100246-105100255 chr11:105100244-105100257 chr11:105100244-105100257 chr11:105100246-105100255 chr11:105100246-105100255
46	CEBPB	chr11:105051852-105052628	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr11:105115154-105115582	IMR90	lung:	n/a	n/a
48	CEBPB	chr11:105060375-105060656	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr11:105022935-105023276	HepG2	liver:	n/a	chr11:105023107-105023118 chr11:105023123-105023134
50	CEBPB	chr11:105114894-105115596	Hela-S3	cervix:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:105022900-105022950	AG09319	gingival:	n/a
2	chr11:105096701-105096751	SAEC	small airway:	n/a
3	chr11:105022900-105022950	SAEC	small airway:	n/a
4	chr11:105022900-105022950	AG04449	skin:	fetal
5	chr11:105096701-105096751	Caco-2	colon:	n/a
6	chr11:105096701-105096751	PFSK-1	brain:	n/a
7	chr11:105096701-105096751	BE2_C	brain:	n/a
8	chr11:105096701-105096751	NT2-D1	testis:	n/a
9	chr11:105096701-105096751	SK-N-SH	brain:	n/a
10	chr11:105022900-105022950	GM12891	blood:	n/a
11	chr11:105022900-105022950	HIPEpiC	eye:	n/a
12	chr11:105022900-105022950	BE2_C	brain:	n/a
13	chr11:105096701-105096751	RPTEC	kidney:	n/a
14	chr11:105096701-105096751	HUVEC	blood vessel:	n/a
15	chr11:105022900-105022950	RPTEC	kidney:	n/a
16	chr11:105096701-105096751	NHDF-neo	bronchial:	n/a
17	chr11:105022900-105022950	MCF-7	breast:	n/a
18	chr11:105022900-105022950	BJ	skin:	n/a
19	chr11:105022900-105022950	HMEC	breast:	n/a
20	chr11:105096701-105096751	Hepatocyte	liver:	n/a
21	chr11:105022900-105022950	T-47D	breast:	n/a
22	chr11:105096701-105096751	HRE	kidney:	n/a
23	chr11:105096701-105096751	HCPEpiC	choroid plexus:	n/a
24	chr11:105096701-105096751	HL-60	blood:	n/a
25	chr11:105022900-105022950	HepG2	liver:	n/a
26	chr11:105022900-105022950	NB4	blood:	n/a
27	chr11:105022900-105022950	GM19239	blood:	n/a
28	chr11:105022900-105022950	SKMC	muscle:	n/a
29	chr11:105096701-105096751	MCF-7	breast:	n/a
30	chr11:105096701-105096751	HRPEpiC	eye:	n/a
31	chr11:105022900-105022950	MCF10A-Er-Src	breast:	n/a
32	chr11:105096701-105096751	AG04449	skin:	fetal
33	chr11:105096701-105096751	AG09309	skin:	n/a
34	chr11:105096701-105096751	HCT-116	colon:	n/a
35	chr11:105022900-105022950	GM12878	blood:	n/a
36	chr11:105096701-105096751	HCF	heart:	n/a
37	chr11:105022900-105022950	HPAEpiC	pulmonary alveolar:	n/a
38	chr11:105022900-105022950	HEEpiC	esophagus:	n/a
39	chr11:105096701-105096751	MCF10A-Er-Src	breast:	n/a
40	chr11:105022900-105022950	HAEpiC	amniotic membrane:	n/a
41	chr11:105022900-105022950	NH-A	brain:	n/a
42	chr11:105022900-105022950	Hepatocyte	liver:	n/a
43	chr11:105096701-105096751	HRCEpiC	kidney:	n/a
44	chr11:105096701-105096751	ProgFib	skin:	n/a
45	chr11:105022900-105022950	H1-hESC	embryonic stem cell:	embryo
46	chr11:105022900-105022950	PANC-1	pancreas:	n/a
47	chr11:105022900-105022950	HCT-116	colon:	n/a
48	chr11:105096701-105096751	GM19239	blood:	n/a
49	chr11:105022900-105022950	HCM	heart:	n/a
50	chr11:105022900-105022950	GM06990	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:105056257..105058944-chr11:105060943..105064813,3	K562	blood:
2	chr11:105114147..105114647-chr9:140135285..140136197,2	Hela-S3	cervix:
3	chr11:105081391..105083161-chr11:105086311..105088202,2	MCF-7	breast:
4	chr11:105125650..105127473-chr11:105130695..105132691,2	K562	blood:
5	chr11:105079428..105081652-chr11:105083843..105086714,2	K562	blood:
6	chr11:105056257..105058944-chr11:105060943..105064813,3	K562	blood:
7	chr11:105039682..105042328-chr11:105072015..105073951,2	K562	blood:
8	chr11:105039682..105042328-chr11:105072015..105073951,2	K562	blood:
9	chr11:105079428..105081652-chr11:105083843..105086714,2	K562	blood:
10	chr11:105125650..105127473-chr11:105130695..105132691,2	K562	blood:
11	chr11:105081391..105083161-chr11:105086311..105088202,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CARD18-2	chr11:105030992-105031083	ENSG00000254998.1
2	lnc-CARD18-4	chr11:105065167-105065673	NONHSAT023956
3	lnc-CARD18-2	chr11:105028654-105028817	ENSG00000254998.1
4	lnc-CARD18-2	chr11:105130369-105130412	ENSG00000254998.1

Variant related genes	Relation type
OR2AL1P	TF binding region
ENSG00000255336	TF binding region
OR2AL1P	CpG island
ENSG00000255336	CpG island
ENSG00000188229	chromatin interactions

Extended variants
information (count: 3581 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:3581 , 50 per page) page: 1 2 3 4 5 6 7 ... 72

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs554205720	chr11:105016013-105016014	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs532125159	chr11:105016017-105016018	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs569279987	chr11:105016035-105016036	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs377601027	chr11:105016055-105016056	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs547530716	chr11:105016100-105016101	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs559285307	chr11:105016137-105016138	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs1354323	chr11:105016141-105016142	Enhancers Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs372203591	chr11:105016144-105016145	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs184918601	chr11:105016151-105016152	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs558266168	chr11:105016181-105016182	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs569999148	chr11:105016182-105016183	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs578019031	chr11:105016203-105016204	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs530902402	chr11:105016215-105016216	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs113390224	chr11:105016230-105016231	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs375067157	chr11:105016263-105016264	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs1503397	chr11:105016299-105016300	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs553480539	chr11:105016321-105016322	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs117224310	chr11:105016357-105016358	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs371454029	chr11:105016359-105016360	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs542096616	chr11:105016388-105016389	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs371998770	chr11:105016389-105016390	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs1503398	chr11:105016397-105016398	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs557211982	chr11:105016401-105016402	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs55927429	chr11:105016447-105016448	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs187839402	chr11:105016461-105016462	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs112111466	chr11:105016462-105016463	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs558279532	chr11:105016469-105016470	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs79104403	chr11:105016476-105016477	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs540765969	chr11:105016528-105016529	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs147687923	chr11:105016557-105016558	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs529834397	chr11:105016575-105016576	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs542073023	chr11:105016576-105016577	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs117380219	chr11:105016610-105016611	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs530839798	chr11:105016643-105016644	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs192759045	chr11:105016703-105016704	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs7943658	chr11:105016716-105016717	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs7943758	chr11:105016759-105016760	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs142363432	chr11:105016766-105016767	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs568570439	chr11:105016797-105016798	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs144632799	chr11:105016803-105016804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs7943776	chr11:105016817-105016818	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs7925360	chr11:105016834-105016835	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs117161942	chr11:105016859-105016860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs572805371	chr11:105016863-105016864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs139375718	chr11:105016875-105016876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs372196031	chr11:105016876-105016877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs372585478	chr11:105016885-105016886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs7943892	chr11:105016907-105016908	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs7925579	chr11:105016958-105016959	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs541055806	chr11:105017007-105017008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:97)

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
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	17142309	CNVD

Chromatin state (count:412 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:105010600-105026400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr11:105013200-105016000	Enhancers	HUVEC	blood vessel
3	chr11:105015200-105016000	Enhancers	HMEC	breast
4	chr11:105015200-105016400	Enhancers	NHLF	lung
5	chr11:105015200-105016600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr11:105015400-105016000	Enhancers	NH-A	brain
7	chr11:105015600-105016000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr11:105015600-105016000	Enhancers	NHDF-Ad	bronchial
9	chr11:105015600-105016000	Enhancers	NHEK	skin
10	chr11:105015600-105016200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr11:105015600-105016400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr11:105015600-105016600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr11:105015600-105016600	Enhancers	Hela-S3	cervix
14	chr11:105015800-105016000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
15	chr11:105015800-105016200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr11:105015800-105016400	Enhancers	Rectal Mucosa Donor 31	rectum
17	chr11:105015800-105016600	Enhancers	Duodenum Mucosa	Duodenum
18	chr11:105015800-105016600	Enhancers	Fetal Intestine Large	intestine
19	chr11:105015800-105016600	Enhancers	HepG2	liver
20	chr11:105015800-105016800	Enhancers	Fetal Intestine Small	intestine
21	chr11:105016000-105016200	Active TSS	Muscle Satellite Cultured Cells	--
22	chr11:105016000-105022800	Weak transcription	NH-A	brain
23	chr11:105016400-105016600	Enhancers	Esophagus	oesophagus
24	chr11:105016600-105023400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr11:105022400-105022600	Weak transcription	Hela-S3	cervix
26	chr11:105022400-105023600	Enhancers	HUVEC	blood vessel
27	chr11:105022400-105024000	Enhancers	Muscle Satellite Cultured Cells	--
28	chr11:105022600-105024400	Enhancers	Hela-S3	cervix
29	chr11:105022800-105023000	Enhancers	NH-A	brain
30	chr11:105023000-105023400	Flanking Active TSS	NH-A	brain
31	chr11:105023000-105023600	Enhancers	Monocytes-CD14+_RO01746	blood
32	chr11:105023400-105023600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr11:105023400-105023600	Enhancers	NH-A	brain
34	chr11:105023400-105024000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr11:105023400-105024400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr11:105023600-105026400	Weak transcription	HUVEC	blood vessel
37	chr11:105023800-105024400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr11:105023800-105024400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr11:105024000-105024400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr11:105026000-105027800	Enhancers	Breast Myoepithelial Primary Cells	Breast
41	chr11:105026400-105027200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr11:105026400-105027600	Enhancers	HUVEC	blood vessel
43	chr11:105026600-105027200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
44	chr11:105026800-105027800	Enhancers	Primary neutrophils fromperipheralblood	blood
45	chr11:105027000-105027800	Enhancers	Placenta	Placenta
46	chr11:105027800-105029000	Weak transcription	Primary neutrophils fromperipheralblood	blood
47	chr11:105029000-105029400	Enhancers	Monocytes-CD14+_RO01746	blood
48	chr11:105029000-105029600	Enhancers	Primary monocytes fromperipheralblood	blood
49	chr11:105029000-105030000	Enhancers	Primary neutrophils fromperipheralblood	blood
50	chr11:105033600-105034600	Enhancers	HUVEC	blood vessel

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