Variant report

Variant	nsv820117
Chromosome Location	chr12:43019570-43027481
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	CEBPB	chr12:43025345-43025677	IMR90	lung:	n/a	n/a
2	CEBPB	chr12:43025330-43025600	K562	blood:	n/a	n/a
3	CEBPB	chr12:43025322-43025688	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr12:43025444-43025655	A549	lung:	n/a	n/a
5	CEBPB	chr12:43025359-43025674	H1-hESC	embryonic stem cell:	n/a	n/a
6	CHD2	chr12:43019491-43019597	K562	blood:	n/a	n/a
7	EP300	chr12:43024204-43024416	K562	blood:	n/a	n/a
8	EP300	chr12:43025398-43025636	Hela-S3	cervix:	n/a	n/a
9	KAP1	chr12:43023782-43024522	U2OS	brain:	n/a	n/a
10	KAP1	chr12:43023607-43024511	HEK293	kidney:	n/a	n/a
11	MAZ	chr12:43027324-43027341	HepG2	liver:	n/a	n/a
12	NFIC	chr12:43019321-43019865	ECC-1	luminal epithelium:	n/a	n/a
13	NFYA	chr12:43019481-43019684	Hela-S3	cervix:	n/a	chr12:43019530-43019548 chr12:43019554-43019572
14	NFYA	chr12:43019379-43019678	K562	blood:	n/a	chr12:43019530-43019548 chr12:43019554-43019572
15	NFYB	chr12:43019303-43019703	K562	blood:	n/a	chr12:43019560-43019575 chr12:43019536-43019551 chr12:43019512-43019527
16	NFYB	chr12:43019379-43019617	GM12878	blood:	n/a	chr12:43019560-43019575 chr12:43019536-43019551 chr12:43019512-43019527
17	NFYB	chr12:43019394-43019613	Hela-S3	cervix:	n/a	chr12:43019560-43019575 chr12:43019536-43019551 chr12:43019512-43019527
18	POLR2A	chr12:43023525-43023576	GM12878	blood:	n/a	n/a
19	POLR2A	chr12:43026076-43026105	MCF10A-Er-Src	breast:	n/a	n/a
20	POLR2A	chr12:43023607-43023620	MCF10A-Er-Src	breast:	n/a	n/a
21	PRDM1	chr12:43025419-43025709	Hela-S3	cervix:	n/a	chr12:43025547-43025561 chr12:43025548-43025561 chr12:43025548-43025557 chr12:43025464-43025479
22	RCOR1	chr12:43024116-43024461	K562	blood:	n/a	n/a
23	SETDB1	chr12:43023947-43024926	U2OS	brain:	n/a	n/a
24	SPI1	chr12:43025453-43025798	HL-60	blood:	n/a	n/a
25	STAT3	chr12:43025541-43025741	MCF10A-Er-Src	breast:	n/a	n/a
26	TAL1	chr12:43024297-43024443	K562	blood:	n/a	n/a
27	TCF7L2	chr12:43023886-43024538	HEK293	kidney:	n/a	n/a
28	TEAD4	chr12:43024071-43024481	K562	blood:	n/a	n/a
29	ZNF384	chr12:43024570-43024588	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:43018191..43020196-chr12:43021950..43023568,2	K562	blood:
2	chr12:43020347..43023127-chr12:43029388..43031746,2	K562	blood:
3	chr12:43018191..43020196-chr12:43021950..43023568,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRICKLE1-1	chr12:43023263-43023488	ENSG00000257510

Variant related genes	Relation type
ENSG00000257687	TF binding region
ENSG00000257405	chromatin interactions
POGZ	miRNA target sites

Extended variants
information (count: 294 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:294 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12424138	chr12:43019593-43019594	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs151020738	chr12:43019595-43019596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs56836086	chr12:43019607-43019608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs397975480	chr12:43019609-43019610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs536227354	chr12:43019617-43019618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs182679284	chr12:43019686-43019687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs113032841	chr12:43019755-43019756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs7977195	chr12:43019780-43019781	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs12426988	chr12:43019781-43019782	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs557852588	chr12:43019799-43019800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs186629590	chr12:43019828-43019829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs12424455	chr12:43019872-43019873	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs144720281	chr12:43019984-43019985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs370167943	chr12:43019995-43019996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs143607649	chr12:43020076-43020077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs10880332	chr12:43020166-43020167	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs148047695	chr12:43020167-43020168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs79604310	chr12:43020234-43020235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs545909287	chr12:43020244-43020245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs140881070	chr12:43020274-43020275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs531490403	chr12:43020275-43020276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs150303009	chr12:43020430-43020431	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs386762533	chr12:43020444-43020445	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs77568420	chr12:43020451-43020452	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs538738817	chr12:43020470-43020471	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs150203082	chr12:43020524-43020525	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs191481631	chr12:43020533-43020534	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs184793404	chr12:43020549-43020550	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs547404930	chr12:43020560-43020561	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs566525469	chr12:43020612-43020613	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs78474830	chr12:43020619-43020620	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs7313926	chr12:43020633-43020634	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs139018072	chr12:43020666-43020667	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs538026362	chr12:43020670-43020671	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs79127723	chr12:43020705-43020706	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs113689305	chr12:43020709-43020710	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs536122370	chr12:43020732-43020733	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs143136972	chr12:43020789-43020790	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs17091505	chr12:43020797-43020798	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs202197719	chr12:43020805-43020806	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs147475403	chr12:43020812-43020813	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs12322671	chr12:43020819-43020820	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs373992491	chr12:43020825-43020826	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs7302424	chr12:43020849-43020850	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs189167570	chr12:43020856-43020857	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs192872508	chr12:43020857-43020858	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs7131974	chr12:43020864-43020865	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs118070832	chr12:43020879-43020880	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs80034683	chr12:43020889-43020890	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs527632703	chr12:43020915-43020916	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Seminomas	18059402	CNVD
Wilms tumour	21544195	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
Ewing''s sarcoma	21437220	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
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Cancer	21183584	CNVD
Hirschsprung''s Disease	21712996	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	20016488	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Acute lymphoblastic leukemia	21339820	CNVD

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:43017000-43020800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr12:43020800-43021000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr12:43020800-43021200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr12:43021000-43021800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr12:43021400-43022000	Enhancers	Fetal Stomach	stomach
6	chr12:43024400-43026200	Enhancers	Monocytes-CD14+_RO01746	blood
7	chr12:43024800-43026000	Enhancers	Primary monocytes fromperipheralblood	blood
8	chr12:43025000-43026000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr12:43025200-43025600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr12:43025200-43026000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr12:43025200-43026600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr12:43025600-43026000	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr12:43025600-43029400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr12:43025800-43026200	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr12:43026000-43029400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links