Variant report

Variant	nsv467741
Chromosome Location	chr11:23781534-23944659
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	chr11:23808741-23808892	HepG2	liver:	n/a	n/a
2	BACH1	chr11:23878232-23878445	H1-hESC	embryonic stem cell:	n/a	n/a
3	BRCA1	chr11:23791141-23791164	Hela-S3	cervix:	n/a	n/a
4	BRCA1	chr11:23924606-23925059	Hela-S3	cervix:	n/a	n/a
5	BRCA1	chr11:23895497-23895518	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr11:23883263-23883345	H1-hESC	embryonic stem cell:	n/a	chr11:23883330-23883341 chr11:23883331-23883340 chr11:23883331-23883340 chr11:23883331-23883340 chr11:23883329-23883340 chr11:23883331-23883340
7	CEBPB	chr11:23876059-23876251	IMR90	lung:	n/a	n/a
8	CEBPB	chr11:23820772-23821109	A549	lung:	n/a	n/a
9	CEBPB	chr11:23808790-23808947	HepG2	liver:	n/a	chr11:23808906-23808917
10	CEBPB	chr11:23891244-23891591	HepG2	liver:	n/a	n/a
11	CEBPB	chr11:23887264-23887584	MCF-7	breast:	n/a	n/a
12	CEBPB	chr11:23883188-23883494	HepG2	liver:	n/a	chr11:23883330-23883341 chr11:23883331-23883340 chr11:23883331-23883340 chr11:23883331-23883340 chr11:23883329-23883340 chr11:23883331-23883340
13	CEBPB	chr11:23878241-23878611	A549	lung:	n/a	chr11:23878381-23878392
14	CEBPB	chr11:23924606-23925075	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr11:23921942-23922265	IMR90	lung:	n/a	chr11:23922112-23922125 chr11:23922112-23922123
16	CEBPB	chr11:23883192-23883491	A549	lung:	n/a	chr11:23883330-23883341 chr11:23883331-23883340 chr11:23883331-23883340 chr11:23883331-23883340 chr11:23883329-23883340 chr11:23883331-23883340
17	CEBPB	chr11:23921978-23922264	HepG2	liver:	n/a	chr11:23922112-23922125 chr11:23922112-23922123
18	CEBPB	chr11:23878225-23878534	HepG2	liver:	n/a	chr11:23878381-23878392
19	CEBPB	chr11:23924628-23925014	IMR90	lung:	n/a	n/a
20	CEBPB	chr11:23876110-23876208	HepG2	liver:	n/a	n/a
21	CEBPB	chr11:23844303-23844514	HepG2	liver:	n/a	chr11:23844394-23844405
22	CEBPB	chr11:23844250-23844479	IMR90	lung:	n/a	chr11:23844394-23844405
23	CEBPB	chr11:23829111-23829319	K562	blood:	n/a	chr11:23829233-23829244
24	CEBPB	chr11:23829075-23829384	HepG2	liver:	n/a	chr11:23829233-23829244
25	CEBPB	chr11:23891235-23891626	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr11:23878231-23878550	A549	lung:	n/a	chr11:23878381-23878392
27	CEBPB	chr11:23891315-23891609	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr11:23820766-23821130	IMR90	lung:	n/a	chr11:23821104-23821117
29	CEBPB	chr11:23891258-23891626	A549	lung:	n/a	n/a
30	CEBPB	chr11:23878236-23878516	MCF-7	breast:	n/a	chr11:23878381-23878392
31	CEBPB	chr11:23944291-23944556	IMR90	lung:	n/a	chr11:23944390-23944401
32	CEBPB	chr11:23891244-23891619	IMR90	lung:	n/a	n/a
33	CEBPB	chr11:23878304-23878551	ECC-1	luminal epithelium:	n/a	chr11:23878381-23878392
34	CEBPB	chr11:23829064-23829390	IMR90	lung:	n/a	chr11:23829233-23829244
35	CEBPB	chr11:23944385-23944494	A549	lung:	n/a	chr11:23944390-23944401
36	CEBPB	chr11:23924608-23925038	A549	lung:	n/a	n/a
37	CEBPB	chr11:23820809-23821124	HepG2	liver:	n/a	chr11:23821104-23821117
38	CEBPB	chr11:23887287-23887522	MCF-7	breast:	n/a	n/a
39	CEBPB	chr11:23883286-23883491	K562	blood:	n/a	chr11:23883330-23883341 chr11:23883331-23883340 chr11:23883331-23883340 chr11:23883331-23883340 chr11:23883329-23883340 chr11:23883331-23883340
40	CEBPB	chr11:23878214-23878526	MCF-7	breast:	n/a	chr11:23878381-23878392
41	CEBPB	chr11:23878299-23878513	A549	lung:	n/a	chr11:23878381-23878392
42	CEBPB	chr11:23878204-23878582	Hela-S3	cervix:	n/a	chr11:23878381-23878392
43	CEBPB	chr11:23944263-23944509	HepG2	liver:	n/a	chr11:23944390-23944401
44	CEBPB	chr11:23921929-23922263	A549	lung:	n/a	chr11:23922112-23922125 chr11:23922112-23922123
45	CEBPB	chr11:23918963-23919709	IMR90	lung:	n/a	chr11:23919170-23919181
46	CEBPB	chr11:23794359-23794613	HepG2	liver:	n/a	chr11:23794482-23794495 chr11:23794482-23794493
47	CEBPB	chr11:23878199-23878609	IMR90	lung:	n/a	chr11:23878381-23878392
48	CEBPB	chr11:23829094-23829349	A549	lung:	n/a	chr11:23829233-23829244
49	CEBPB	chr11:23940961-23941367	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr11:23883174-23883477	IMR90	lung:	n/a	chr11:23883330-23883341 chr11:23883331-23883340 chr11:23883331-23883340 chr11:23883331-23883340 chr11:23883329-23883340 chr11:23883331-23883340

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:23919652-23919702	NHDF-neo	bronchial:	n/a
2	chr11:23811425-23811475	T-47D	breast:	n/a
3	chr11:23926945-23926995	AG09309	skin:	n/a
4	chr11:23919652-23919702	RPTEC	kidney:	n/a
5	chr11:23919652-23919702	GM19239	blood:	n/a
6	chr11:23919652-23919702	MCF-7	breast:	n/a
7	chr11:23919652-23919702	SKMC	muscle:	n/a
8	chr11:23926945-23926995	PANC-1	pancreas:	n/a
9	chr11:23811425-23811475	LNCaP	prostate:	n/a
10	chr11:23895772-23895822	HCM	heart:	n/a
11	chr11:23919652-23919702	PANC-1	pancreas:	n/a
12	chr11:23811425-23811475	AG04450	lung:	fetal
13	chr11:23926945-23926995	HEEpiC	esophagus:	n/a
14	chr11:23919652-23919702	AG04450	lung:	fetal
15	chr11:23811425-23811475	HCM	heart:	n/a
16	chr11:23926945-23926995	BE2_C	brain:	n/a
17	chr11:23895772-23895822	A549	lung:	n/a
18	chr11:23919652-23919702	HL-60	blood:	n/a
19	chr11:23919652-23919702	GM12891	blood:	n/a
20	chr11:23895772-23895822	GM12878	blood:	n/a
21	chr11:23811425-23811475	K562	blood:	n/a
22	chr11:23811425-23811475	HCF	heart:	n/a
23	chr11:23811425-23811475	PANC-1	pancreas:	n/a
24	chr11:23926945-23926995	AG04449	skin:	fetal
25	chr11:23811425-23811475	MCF-7	breast:	n/a
26	chr11:23926945-23926995	LNCaP	prostate:	n/a
27	chr11:23919652-23919702	IMR90	lung:	fetal
28	chr11:23895772-23895822	MCF10A-Er-Src	breast:	n/a
29	chr11:23811425-23811475	HMEC	breast:	n/a
30	chr11:23919652-23919702	AoSMC	blood vessel:	n/a
31	chr11:23895772-23895822	SK-N-MC	brain:	n/a
32	chr11:23895772-23895822	HCF	heart:	n/a
33	chr11:23895772-23895822	HPAEpiC	pulmonary alveolar:	n/a
34	chr11:23811425-23811475	IMR90	lung:	fetal
35	chr11:23811425-23811475	GM12892	blood:	n/a
36	chr11:23926945-23926995	HNPCEpiC	eye:	n/a
37	chr11:23919652-23919702	HCT-116	colon:	n/a
38	chr11:23926945-23926995	SAEC	small airway:	n/a
39	chr11:23919652-23919702	NB4	blood:	n/a
40	chr11:23895772-23895822	NHDF-neo	bronchial:	n/a
41	chr11:23811425-23811475	PrEC	prostate:	n/a
42	chr11:23895772-23895822	HRCEpiC	kidney:	n/a
43	chr11:23895772-23895822	HMEC	breast:	n/a
44	chr11:23919652-23919702	Caco-2	colon:	n/a
45	chr11:23926945-23926995	SK-N-MC	brain:	n/a
46	chr11:23926945-23926995	HRE	kidney:	n/a
47	chr11:23919652-23919702	T-47D	breast:	n/a
48	chr11:23919652-23919702	U87	brain:	n/a
49	chr11:23926945-23926995	PFSK-1	brain:	n/a
50	chr11:23811425-23811475	BJ	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:23822728..23824994-chr11:23830826..23833587,2	K562	blood:
2	chr11:23798376..23799116-chr5:32449587..32450235,2	MCF-7	breast:
3	chr11:23822728..23824994-chr11:23830826..23833587,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-17A1.2.1-5	chr11:23817463-23817487	NONHSAT018430
2	lnc-LUZP2-1	chr11:23818254-23818516	ENSG00000255193
3	lnc-RP11-17A1.2.1-2	chr11:23829736-23829778	XLOC_009395
4	lnc-RP11-17A1.2.1-5	chr11:23818256-23819005	NONHSAT018430
5	lnc-LUZP2-3	chr11:23908634-23908905	NONHSAT018434
6	lnc-RP11-17A1.2.1-2	chr11:23826000-23826222	XLOC_009395
7	lnc-LUZP2-1	chr11:23816369-23816430	ENSG00000255193
8	lnc-RP11-17A1.2.1-2	chr11:23782876-23783176	ENSG00000254861
9	lnc-RP11-17A1.2.1-6	chr11:23877391-23877541	NONHSAT018433
10	lnc-RP11-17A1.2.1-2	chr11:23782899-23783176	XLOC_009394
11	lnc-RP11-17A1.2.1-2	chr11:23802334-23802418	ENSG00000254861
12	lnc-RP11-17A1.2.1-2	chr11:23826025-23826144	ENSG00000254861
13	lnc-RP11-17A1.2.1-6	chr11:23874839-23875216	NONHSAT018433
14	lnc-RP11-17A1.2.1-2	chr11:23789323-23789362	XLOC_009394
15	lnc-LUZP2-3	chr11:23911055-23911129	NONHSAT018434

Variant related genes	Relation type
RNU6-783P	TF binding region
ENSG00000254861	TF binding region
RNU6-783P	CpG island
ENSG00000254861	CpG island

Extended variants
information (count: 3921 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:3921 , 50 per page) page: 1 2 3 4 5 6 7 ... 79

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7116643	chr11:23781534-23781535	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs192217739	chr11:23781576-23781577	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs75007796	chr11:23781579-23781580	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs76878357	chr11:23781623-23781624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs184779338	chr11:23781624-23781625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs539224143	chr11:23781695-23781696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs558671882	chr11:23781699-23781700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs575324679	chr11:23781768-23781769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs544603062	chr11:23781769-23781770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs561078610	chr11:23781783-23781784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs574975182	chr11:23781868-23781869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs371381690	chr11:23781948-23781949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs372242143	chr11:23781959-23781960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs560749729	chr11:23781981-23781982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs532783577	chr11:23781994-23781995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs187987160	chr11:23782038-23782039	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs115883546	chr11:23782054-23782055	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs562615888	chr11:23782059-23782060	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs73439894	chr11:23782072-23782073	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs548171833	chr11:23782078-23782079	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs567937037	chr11:23782082-23782083	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs541215625	chr11:23782108-23782109	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs559665287	chr11:23782132-23782133	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs568000886	chr11:23782145-23782146	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs570409570	chr11:23782181-23782182	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs535308959	chr11:23782205-23782206	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs577893920	chr11:23782255-23782256	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs539288834	chr11:23782319-23782320	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs192552705	chr11:23782328-23782329	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs184299632	chr11:23782426-23782427	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs188330241	chr11:23782434-23782435	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs78838135	chr11:23782523-23782524	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs181801285	chr11:23782528-23782529	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs540597101	chr11:23782539-23782540	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs554554924	chr11:23782547-23782548	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs79274483	chr11:23782583-23782584	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs74576209	chr11:23782584-23782585	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs11027484	chr11:23782637-23782638	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs184811726	chr11:23782654-23782655	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs73439896	chr11:23782693-23782694	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs112580692	chr11:23782762-23782763	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs561806335	chr11:23782832-23782833	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs527341983	chr11:23782873-23782874	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs188813985	chr11:23782877-23782878	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
45	rs149678527	chr11:23782882-23782883	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
46	rs550822773	chr11:23782886-23782887	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
47	rs533011241	chr11:23782942-23782943	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
48	rs61876077	chr11:23782952-23782953	Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs563545704	chr11:23782974-23782975	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
50	rs181816660	chr11:23783008-23783009	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
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
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Multiple myeloma	16461302	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Medulloblastoma	16783165	CNVD
small cell lung cancer	20016488	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Renal cell carcinoma	18194544	CNVD
Myelofibrosis	22110671	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
Chordoma	18071362	CNVD
Autism	22102821	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21364760	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:275 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:23772400-23782400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr11:23781400-23785400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr11:23781400-23787200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
4	chr11:23782000-23783200	Enhancers	Fetal Lung	lung
5	chr11:23782400-23783200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr11:23785400-23789000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr11:23786200-23786400	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr11:23787000-23788200	Enhancers	Placenta Amnion	Placenta Amnion
9	chr11:23787200-23788000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr11:23787200-23788000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr11:23787200-23788200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
12	chr11:23789200-23792000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr11:23790200-23791200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
14	chr11:23790400-23791800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
15	chr11:23792600-23794200	Enhancers	Fetal Stomach	stomach
16	chr11:23792800-23794200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr11:23794200-23795200	Weak transcription	Fetal Stomach	stomach
18	chr11:23795200-23795400	Enhancers	Fetal Stomach	stomach
19	chr11:23798600-23799200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr11:23799200-23803200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr11:23799600-23802400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr11:23800400-23802000	Enhancers	NH-A	brain
23	chr11:23800600-23802600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr11:23800800-23801200	Enhancers	HSMM	muscle
25	chr11:23801200-23811000	Weak transcription	HSMM	muscle
26	chr11:23803200-23803600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr11:23803600-23804600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr11:23804600-23806800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr11:23805200-23806400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr11:23805800-23806200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr11:23806200-23811200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr11:23806400-23806600	Enhancers	Sigmoid Colon	Sigmoid Colon
33	chr11:23806400-23807000	Enhancers	HepG2	liver
34	chr11:23806600-23806800	Enhancers	Rectal Mucosa Donor 31	rectum
35	chr11:23806800-23808200	Weak transcription	Rectal Mucosa Donor 31	rectum
36	chr11:23806800-23808200	Weak transcription	Sigmoid Colon	Sigmoid Colon
37	chr11:23807000-23808000	Weak transcription	HepG2	liver
38	chr11:23807000-23809000	Enhancers	Fetal Intestine Small	intestine
39	chr11:23807400-23808600	Enhancers	Fetal Lung	lung
40	chr11:23807800-23809400	Enhancers	Stomach Mucosa	stomach
41	chr11:23808000-23809400	Enhancers	Fetal Intestine Large	intestine
42	chr11:23808000-23809600	Enhancers	HepG2	liver
43	chr11:23808200-23809000	Enhancers	Gastric	stomach
44	chr11:23808200-23809000	Enhancers	Sigmoid Colon	Sigmoid Colon
45	chr11:23808200-23809600	Enhancers	Rectal Mucosa Donor 31	rectum
46	chr11:23808800-23809000	Enhancers	Pancreas	Pancrea
47	chr11:23809000-23810600	Weak transcription	Fetal Intestine Small	intestine
48	chr11:23809000-23810600	Weak transcription	Sigmoid Colon	Sigmoid Colon
49	chr11:23809400-23810600	Weak transcription	Fetal Intestine Large	intestine
50	chr11:23809400-23810600	Weak transcription	Pancreas	Pancrea

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