Variant report

Variant	nsv470275
Chromosome Location	chr12:21938544-22126314
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:685)
CpG islands
(count:1405)
Chromatin interactive
region (count:33)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:685 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:21979519-21979803	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:21972129-21972499	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:22094968-22095091	HepG2	liver:	n/a	n/a
4	ARID3A	chr12:21966004-21966439	K562	blood:	n/a	chr12:21966149-21966165
5	ARID3A	chr12:21967124-21967686	HepG2	liver:	n/a	n/a
6	BACH1	chr12:21984990-21985085	K562	blood:	n/a	n/a
7	BACH1	chr12:22095180-22095347	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr12:21962535-21962560	K562	blood:	n/a	n/a
9	BCL11A	chr12:21948880-21949139	GM12878	blood:	n/a	chr12:21949064-21949073
10	BCL3	chr12:22029750-22030211	GM12878	blood:	n/a	n/a
11	BCL3	chr12:21948880-21949188	GM12878	blood:	n/a	chr12:21949064-21949073
12	CBX3	chr12:22099915-22100287	K562	blood:	n/a	n/a
13	CBX3	chr12:22099955-22100205	K562	blood:	n/a	n/a
14	CCNT2	chr12:21966038-21966426	K562	blood:	n/a	n/a
15	CEBPB	chr12:22007441-22007666	Hela-S3	cervix:	n/a	chr12:22007537-22007548
16	CEBPB	chr12:22006283-22006286	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr12:22115139-22115495	IMR90	lung:	n/a	n/a
18	CEBPB	chr12:22032265-22032611	Hela-S3	cervix:	n/a	chr12:22032431-22032442 chr12:22032466-22032477 chr12:22032398-22032409
19	CEBPB	chr12:22032280-22032629	A549	lung:	n/a	chr12:22032431-22032442 chr12:22032466-22032477 chr12:22032398-22032409
20	CEBPB	chr12:22007413-22007704	IMR90	lung:	n/a	chr12:22007537-22007548
21	CEBPB	chr12:22064893-22065547	IMR90	lung:	n/a	chr12:22065069-22065080
22	CEBPB	chr12:22045711-22046062	K562	blood:	n/a	chr12:22045894-22045905
23	CEBPB	chr12:22045760-22046074	H1-hESC	embryonic stem cell:	n/a	chr12:22045894-22045905
24	CEBPB	chr12:22064865-22065268	K562	blood:	n/a	chr12:22065069-22065080
25	CEBPB	chr12:22045721-22046065	HepG2	liver:	n/a	chr12:22045894-22045905
26	CEBPB	chr12:22073853-22074012	IMR90	lung:	n/a	n/a
27	CEBPB	chr12:22124459-22124574	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr12:22005186-22005550	IMR90	lung:	n/a	n/a
29	CEBPB	chr12:22007376-22007632	HepG2	liver:	n/a	chr12:22007537-22007548
30	CEBPB	chr12:22064894-22065168	K562	blood:	n/a	chr12:22065069-22065080
31	CEBPB	chr12:22045726-22046083	IMR90	lung:	n/a	chr12:22045894-22045905
32	CEBPB	chr12:22064922-22065195	HepG2	liver:	n/a	chr12:22065069-22065080
33	CEBPB	chr12:21966136-21966389	K562	blood:	n/a	n/a
34	CEBPB	chr12:21976813-21976868	K562	blood:	n/a	n/a
35	CEBPB	chr12:22045722-22046065	A549	lung:	n/a	chr12:22045894-22045905
36	CEBPB	chr12:22047836-22047955	HepG2	liver:	n/a	chr12:22047875-22047886 chr12:22047874-22047887
37	CEBPB	chr12:22091880-22092220	K562	blood:	n/a	chr12:22092050-22092061 chr12:22092051-22092062
38	CEBPB	chr12:21949278-21949529	A549	lung:	n/a	chr12:21949340-21949351
39	CEBPB	chr12:22006117-22006317	HepG2	liver:	n/a	chr12:22006214-22006225
40	CEBPB	chr12:22006171-22006369	K562	blood:	n/a	chr12:22006214-22006225
41	CEBPB	chr12:22007495-22007635	A549	lung:	n/a	chr12:22007537-22007548
42	CEBPB	chr12:21981738-21982073	MCF-7	breast:	n/a	n/a
43	CEBPB	chr12:22091911-22092187	HepG2	liver:	n/a	chr12:22092050-22092061 chr12:22092051-22092062
44	CEBPB	chr12:21949266-21949534	HepG2	liver:	n/a	chr12:21949340-21949351
45	CEBPB	chr12:22032317-22032587	MCF-7	breast:	n/a	chr12:22032431-22032442 chr12:22032466-22032477 chr12:22032398-22032409
46	CEBPB	chr12:22091880-22092235	IMR90	lung:	n/a	chr12:22092050-22092061 chr12:22092051-22092062
47	CEBPB	chr12:22007378-22007571	K562	blood:	n/a	chr12:22007537-22007548
48	CEBPB	chr12:22032366-22032566	K562	blood:	n/a	chr12:22032431-22032442 chr12:22032466-22032477 chr12:22032398-22032409
49	CEBPB	chr12:22045714-22046097	A549	lung:	n/a	chr12:22045894-22045905
50	CEBPB	chr12:21981315-21982058	IMR90	lung:	n/a	n/a

(count:1405 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:22093960-22094010	SAEC	small airway:	n/a
2	chr12:22095182-22095232	NHDF-neo	bronchial:	n/a
3	chr12:22093960-22094010	SAEC	small airway:	n/a
4	chr12:22095182-22095232	NHDF-neo	bronchial:	n/a
5	chr12:22094479-22094529	ECC-1	luminal epithelium:	n/a
6	chr12:22124437-22124487	HepG2	liver:	n/a
7	chr12:22094371-22094421	AG09319	gingival:	n/a
8	chr12:22093960-22094010	HAEpiC	amniotic membrane:	n/a
9	chr12:22095477-22095527	HPAEpiC	pulmonary alveolar:	n/a
10	chr12:22094461-22094511	H1-hESC	embryonic stem cell:	embryo
11	chr12:22094699-22094749	SK-N-SH_RA	brain:	n/a
12	chr12:22094750-22094800	GM12878	blood:	n/a
13	chr12:22099120-22099170	HAEpiC	amniotic membrane:	n/a
14	chr12:22094563-22094613	ECC-1	luminal epithelium:	n/a
15	chr12:22093960-22094010	A549	lung:	n/a
16	chr12:22090730-22090780	HRCEpiC	kidney:	n/a
17	chr12:22094034-22094084	H1-hESC	embryonic stem cell:	embryo
18	chr12:22093960-22094010	PANC-1	pancreas:	n/a
19	chr12:22090231-22090281	GM06990	blood:	n/a
20	chr12:22095477-22095527	SK-N-SH_RA	brain:	n/a
21	chr12:22090231-22090281	NH-A	brain:	n/a
22	chr12:22090231-22090281	AG04449	skin:	fetal
23	chr12:22094371-22094421	Caco-2	colon:	n/a
24	chr12:22095111-22095161	IMR90	lung:	fetal
25	chr12:22090730-22090780	HNPCEpiC	eye:	n/a
26	chr12:22095182-22095232	HCF	heart:	n/a
27	chr12:22021295-22021345	ovcar-3	ovarian:	n/a
28	chr12:22094699-22094749	Hepatocyte	liver:	n/a
29	chr12:22099120-22099170	HCF	heart:	n/a
30	chr12:22094226-22094276	GM12891	blood:	n/a
31	chr12:22021295-22021345	H1-hESC	embryonic stem cell:	embryo
32	chr12:22094009-22094059	Caco-2	colon:	n/a
33	chr12:22094750-22094800	HCT-116	colon:	n/a
34	chr12:22089560-22089610	A549	lung:	n/a
35	chr12:22094750-22094800	MCF-7	breast:	n/a
36	chr12:22094750-22094800	CMK	blood:	n/a
37	chr12:22090231-22090281	HAEpiC	amniotic membrane:	n/a
38	chr12:22094226-22094276	SK-N-SH_RA	brain:	n/a
39	chr12:22095182-22095232	HAEpiC	amniotic membrane:	n/a
40	chr12:22094963-22095013	Hela-S3	cervix:	n/a
41	chr12:22124437-22124487	MCF-7	breast:	n/a
42	chr12:22095477-22095527	GM12878	blood:	n/a
43	chr12:22095330-22095380	Hela-S3	cervix:	n/a
44	chr12:22094009-22094059	HL-60	blood:	n/a
45	chr12:22095477-22095527	SK-N-MC	brain:	n/a
46	chr12:22089560-22089610	HCT-116	colon:	n/a
47	chr12:22099120-22099170	HUVEC	blood vessel:	n/a
48	chr12:22095111-22095161	K562	blood:	n/a
49	chr12:22090730-22090780	AoSMC	blood vessel:	n/a
50	chr12:22094750-22094800	HL-60	blood:	n/a

(count:33 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:22077867..22080304-chr12:22090934..22093456,2	K562	blood:
2	chr12:21975085..21976585-chr17:41398734..41400729,2	MCF-7	breast:
3	chr12:22034102..22036993-chr12:22040454..22043984,3	K562	blood:
4	chr12:21925815..21927686-chr12:21953359..21956118,2	K562	blood:
5	chr12:22015594..22017294-chr12:22022518..22025494,2	MCF-7	breast:
6	chr12:22035471..22036993-chr12:22040454..22042900,2	K562	blood:
7	chr12:21928562..21931377-chr12:22097425..22100268,2	K562	blood:
8	chr12:22034102..22036993-chr12:22040454..22043984,3	K562	blood:
9	chr12:22061241..22063260-chr12:22065386..22067190,2	K562	blood:
10	chr12:22106400..22108230-chr12:22109469..22111638,2	MCF-7	breast:
11	chr12:22035471..22036993-chr12:22040454..22042900,2	K562	blood:
12	chr12:22077867..22080304-chr12:22090934..22093456,2	K562	blood:
13	chr12:22106400..22108230-chr12:22109469..22111638,2	MCF-7	breast:
14	chr12:22041351..22043151-chr12:22046321..22048748,2	MCF-7	breast:
15	chr12:22061241..22063351-chr12:22065690..22068312,2	K562	blood:
16	chr12:22100774..22102572-chr12:22104027..22106042,2	MCF-7	breast:
17	chr12:22044149..22046273-chr12:22050074..22052072,2	K562	blood:
18	chr12:22061241..22063351-chr12:22065690..22068312,2	K562	blood:
19	chr12:22041351..22043151-chr12:22046321..22048748,2	MCF-7	breast:
20	chr12:22017240..22019751-chr12:22023346..22025897,2	K562	blood:
21	chr12:22044149..22046273-chr12:22050074..22052072,2	K562	blood:
22	chr12:21958533..21960369-chr12:21961776..21963786,2	K562	blood:
23	chr12:22031693..22034334-chr13:31039008..31041172,2	MCF-7	breast:
24	chr12:22085812..22088348-chr12:22089764..22092154,2	K562	blood:
25	chr12:22061241..22063260-chr12:22065386..22067190,2	K562	blood:
26	chr11:62607619..62609220-chr12:21976585..21978105,2	K562	blood:
27	chr12:22085812..22088348-chr12:22089764..22092154,2	K562	blood:
28	chr12:21958533..21960369-chr12:21961776..21963786,2	K562	blood:
29	chr12:21976585..21978105-chr17:41380641..41383388,2	K562	blood:
30	chr12:22091922..22094311-chr12:22095852..22098312,2	K562	blood:
31	chr12:22017240..22019751-chr12:22023346..22025897,2	K562	blood:
32	chr12:22100774..22102572-chr12:22104027..22106042,2	MCF-7	breast:
33	chr12:22015594..22017294-chr12:22022518..22025494,2	MCF-7	breast:

(count:1 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CMAS-3	chr12:22094338-22097222	NONHSAT027261

No data

Variant related genes	Relation type
ABCC9	TF binding region
ENSG00000257022	TF binding region
ABCC9	CpG island
ENSG00000257022	CpG island
ENSG00000133316	chromatin interactions
ENSG00000069431	chromatin interactions
ENSG00000189403	chromatin interactions
ENSG00000236383	chromatin interactions

Extended variants
information (count: 6245 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:6245 , 50 per page) page: 1 2 3 4 5 6 7 ... 125

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11046186	chr12:21938544-21938545	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs74069162	chr12:21938587-21938588	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs557011687	chr12:21938617-21938618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs573650302	chr12:21938633-21938634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs183848734	chr12:21938676-21938677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs371659982	chr12:21938710-21938711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs188344334	chr12:21938725-21938726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs193017019	chr12:21938781-21938782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs111226426	chr12:21938787-21938788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs184257097	chr12:21938812-21938813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs35408016	chr12:21938835-21938836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs559301855	chr12:21938847-21938848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs144549502	chr12:21938869-21938870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs367764528	chr12:21938969-21938970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs570978243	chr12:21938995-21938996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs12423639	chr12:21938996-21938997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs372657957	chr12:21939027-21939028	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs191553080	chr12:21939044-21939045	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs529206081	chr12:21939058-21939059	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs74069163	chr12:21939062-21939063	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs566156351	chr12:21939079-21939080	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs140736353	chr12:21939103-21939104	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs551934508	chr12:21939112-21939113	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs183696927	chr12:21939116-21939117	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs373303619	chr12:21939117-21939118	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs377558872	chr12:21939154-21939155	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs557640487	chr12:21939166-21939167	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs538608433	chr12:21939214-21939215	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs556794462	chr12:21939215-21939216	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs567277706	chr12:21939246-21939247	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs552044881	chr12:21939267-21939268	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs571795689	chr12:21939281-21939282	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs536242289	chr12:21939288-21939289	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs553148722	chr12:21939315-21939316	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs572871716	chr12:21939328-21939329	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs544911368	chr12:21939353-21939354	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs557667186	chr12:21939375-21939376	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs558734935	chr12:21939379-21939380	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs575320553	chr12:21939427-21939428	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs531137186	chr12:21939486-21939487	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs551156152	chr12:21939576-21939577	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs544107398	chr12:21939578-21939579	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs190811546	chr12:21939596-21939597	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs529289228	chr12:21939600-21939601	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs536660717	chr12:21939631-21939632	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs182049359	chr12:21939638-21939639	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs150093423	chr12:21939665-21939666	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs185535609	chr12:21939708-21939709	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs528599845	chr12:21939739-21939740	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs551553642	chr12:21939747-21939748	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:97)

Disease	PMID	Source
Malignant germ cell tumour	17285132	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Myxofibrosarcoma	16751306	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Acute myeloid leukemia	16864856	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Testicular cancer	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Seminomas	18059402	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Testicular germ cell tumor	18059402	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	16397240	CNVD
Neurodevelopmental disorder	22521361	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	21509527	CNVD
Autism	22102821	CNVD
Follicular lymphoma	18703704	CNVD
Lung cancer	18438408	CNVD
Lung cancer	21911935	CNVD
Breast cancer	22048815	CNVD
Malignant peripheral nerve sheath tumor	19844265	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Heart disease	21282601	CNVD
Ovarian cancer	20844748	CNVD
Lung cancer	17925434	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Gastric cancer	24379144	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Gastric cancer	19545448	CNVD
Lung cancer	20031968	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung adenocarcinoma	19826477	CNVD
Lung cancer	19525976	CNVD
Lung cancer	19826477	CNVD
Non-small cell lung cancer	19451690	CNVD
Non-small cell lung cancer	17504988	CNVD
Bipolar disorder	19114987	CNVD
Lung cancer	19671679	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	21364760	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:1290 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:21929600-21941800	Weak transcription	Pancreas	Pancrea
2	chr12:21939000-21939200	Enhancers	Ovary	ovary
3	chr12:21939000-21939400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr12:21939000-21939800	Enhancers	Adipose Nuclei	Adipose
5	chr12:21939000-21940400	Enhancers	Fetal Lung	lung
6	chr12:21939200-21939400	Enhancers	Aorta	Aorta
7	chr12:21939200-21939400	Enhancers	Fetal Stomach	stomach
8	chr12:21939200-21939600	Flanking Active TSS	Ovary	ovary
9	chr12:21939400-21941000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr12:21939600-21940000	Enhancers	Ovary	ovary
11	chr12:21939800-21941200	Weak transcription	Adipose Nuclei	Adipose
12	chr12:21940000-21940200	Enhancers	Aorta	Aorta
13	chr12:21940000-21940200	Enhancers	Fetal Stomach	stomach
14	chr12:21940000-21941800	Weak transcription	Ovary	ovary
15	chr12:21940400-21940800	Weak transcription	Fetal Lung	lung
16	chr12:21940800-21942000	Enhancers	Fetal Lung	lung
17	chr12:21941000-21941600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr12:21941000-21941800	Enhancers	Liver	Liver
19	chr12:21941200-21941800	Enhancers	Adipose Nuclei	Adipose
20	chr12:21941800-21942000	Enhancers	Ovary	ovary
21	chr12:21941800-21942000	Enhancers	Pancreas	Pancrea
22	chr12:21941800-21957400	Weak transcription	Adipose Nuclei	Adipose
23	chr12:21947800-21948000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr12:21947800-21948000	Enhancers	Stomach Smooth Muscle	stomach
25	chr12:21947800-21949200	Weak transcription	Fetal Heart	heart
26	chr12:21948000-21948600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr12:21948000-21952800	Weak transcription	Liver	Liver
28	chr12:21948000-21957800	Weak transcription	Stomach Smooth Muscle	stomach
29	chr12:21948600-21948800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr12:21948600-21948800	Enhancers	Esophagus	oesophagus
31	chr12:21948800-21950000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr12:21949200-21949400	ZNF genes & repeats	Fetal Heart	heart
33	chr12:21949400-21950800	Enhancers	Fetal Heart	heart
34	chr12:21949600-21961400	Weak transcription	Muscle Satellite Cultured Cells	--
35	chr12:21950000-21954600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr12:21950800-21966200	Weak transcription	Fetal Heart	heart
37	chr12:21951600-21954000	Weak transcription	Skeletal Muscle Female	skeletal muscle
38	chr12:21952400-21956000	Enhancers	Fetal Intestine Large	intestine
39	chr12:21952600-21955800	Enhancers	Fetal Intestine Small	intestine
40	chr12:21952800-21954200	Strong transcription	Liver	Liver
41	chr12:21952800-21955000	Enhancers	Duodenum Mucosa	Duodenum
42	chr12:21953000-21953200	Enhancers	Left Ventricle	heart
43	chr12:21953000-21953400	Enhancers	Pancreatic Islets	Pancreatic Islet
44	chr12:21953200-21957600	Weak transcription	Left Ventricle	heart
45	chr12:21953200-21957600	Weak transcription	Skeletal Muscle Male	skeletal muscle
46	chr12:21953400-21966800	Weak transcription	Pancreatic Islets	Pancreatic Islet
47	chr12:21953400-21971600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr12:21953800-21981000	Weak transcription	Fetal Muscle Trunk	muscle
49	chr12:21954000-21954200	Enhancers	Fetal Kidney	kidney
50	chr12:21954000-21955800	Strong transcription	Skeletal Muscle Female	skeletal muscle

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