Variant report

Variant	nsv983462
Chromosome Location	chr12:46008670-46015543
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	chr12:46008921-46009457	MCF-7	breast:	n/a	chr12:46009043-46009056
2	CEBPB	chr12:46009001-46009362	Hela-S3	cervix:	n/a	chr12:46009043-46009056
3	CHD2	chr12:46009136-46009483	Hela-S3	cervix:	n/a	n/a
4	CTCF	chr12:46009400-46009550	NHDF-neo	bronchial:	n/a	n/a
5	CTCF	chr12:46009620-46009770	HPAF	blood vessel:	n/a	n/a
6	EP300	chr12:46008983-46009502	SK-N-SH	brain:	n/a	chr12:46009237-46009247
7	EP300	chr12:46009066-46009455	SK-N-SH_RA	brain:	n/a	chr12:46009237-46009247
8	EP300	chr12:46009025-46009338	Hela-S3	cervix:	n/a	chr12:46009237-46009247
9	EP300	chr12:46008867-46009547	A549	lung:	n/a	chr12:46009237-46009247
10	EP300	chr12:46008914-46009557	MCF-7	breast:	n/a	chr12:46009237-46009247
11	FOS	chr12:46009160-46009521	Hela-S3	cervix:	n/a	chr12:46009337-46009349 chr12:46009337-46009348 chr12:46009339-46009347
12	FOS	chr12:46009171-46009500	MCF10A-Er-Src	breast:	n/a	chr12:46009337-46009349 chr12:46009337-46009348 chr12:46009339-46009347
13	FOS	chr12:46009176-46009494	MCF10A-Er-Src	breast:	n/a	chr12:46009337-46009349 chr12:46009337-46009348 chr12:46009339-46009347
14	FOS	chr12:46009163-46009498	MCF10A-Er-Src	breast:	n/a	chr12:46009337-46009349 chr12:46009337-46009348 chr12:46009339-46009347
15	FOS	chr12:46008935-46009542	HUVEC	blood vessel:	n/a	chr12:46009337-46009349 chr12:46009337-46009348 chr12:46009339-46009347
16	FOS	chr12:46009170-46009485	MCF10A-Er-Src	breast:	n/a	chr12:46009337-46009349 chr12:46009337-46009348 chr12:46009339-46009347
17	FOSL2	chr12:46009152-46009585	SK-N-SH	brain:	n/a	chr12:46009337-46009349 chr12:46009339-46009347
18	FOSL2	chr12:46009030-46009586	MCF-7	breast:	n/a	chr12:46009337-46009349 chr12:46009339-46009347
19	FOSL2	chr12:46009067-46009540	A549	lung:	n/a	chr12:46009337-46009349 chr12:46009339-46009347
20	FOXA1	chr12:46009167-46009410	T-47D	breast:	n/a	chr12:46009232-46009247
21	FOXA2	chr12:46008952-46009477	A549	lung:	n/a	n/a
22	FOXA2	chr12:46009105-46009470	A549	lung:	n/a	n/a
23	FOXM1	chr12:46008904-46009537	MCF-7	breast:	n/a	n/a
24	FOXM1	chr12:46009006-46009476	MCF-7	breast:	n/a	n/a
25	FOXP2	chr12:46009213-46009384	PFSK-1	brain:	n/a	n/a
26	GATA2	chr12:46009063-46009435	HUVEC	blood vessel:	n/a	chr12:46009340-46009349
27	GATA3	chr12:46008796-46009466	A549	lung:	n/a	chr12:46008935-46008945 chr12:46009340-46009349
28	GATA3	chr12:46009044-46009538	SK-N-SH	brain:	n/a	chr12:46009340-46009349
29	GATA3	chr12:46008815-46009611	MCF-7	breast:	n/a	chr12:46009541-46009552 chr12:46008935-46008945 chr12:46009340-46009349
30	GATA3	chr12:46008746-46009710	MCF-7	breast:	n/a	chr12:46009541-46009552 chr12:46008935-46008945 chr12:46009340-46009349
31	GATA3	chr12:46008948-46009548	SK-N-SH	brain:	n/a	chr12:46009340-46009349
32	HDAC2	chr12:46008959-46009570	MCF-7	breast:	n/a	chr12:46009528-46009542
33	JUN	chr12:46009128-46009450	HUVEC	blood vessel:	n/a	chr12:46009337-46009349 chr12:46009339-46009347
34	JUND	chr12:46009055-46009535	SK-N-SH	brain:	n/a	chr12:46009337-46009349 chr12:46009339-46009347
35	JUND	chr12:46009140-46009493	A549	lung:	n/a	chr12:46009337-46009349 chr12:46009339-46009347
36	JUND	chr12:46009010-46009645	SK-N-SH	brain:	n/a	chr12:46009337-46009349 chr12:46009339-46009347
37	KAP1	chr12:46008973-46009767	U2OS	brain:	n/a	n/a
38	MAX	chr12:46009291-46009335	NB4	blood:	n/a	n/a
39	MYC	chr12:46009256-46009334	Hela-S3	cervix:	n/a	n/a
40	NR2F2	chr12:46008954-46009493	MCF-7	breast:	n/a	n/a
41	PBX3	chr12:46009068-46009522	SK-N-SH	brain:	n/a	n/a
42	PBX3	chr12:46008933-46009572	SK-N-SH	brain:	n/a	n/a
43	POLR2A	chr12:46011754-46011771	MCF-7	breast:	n/a	n/a
44	POLR2A	chr12:46010480-46010514	A549	lung:	n/a	n/a
45	POLR2A	chr12:46008976-46009477	HUVEC	blood vessel:	n/a	n/a
46	POLR2A	chr12:46011812-46011859	MCF-7	breast:	n/a	n/a
47	REST	chr12:46008889-46009414	A549	lung:	n/a	n/a
48	REST	chr12:46009182-46009476	PFSK-1	brain:	n/a	n/a
49	RXRA	chr12:46009061-46009486	SK-N-SH	brain:	n/a	n/a
50	SP1	chr12:46008915-46009492	A549	lung:	n/a	chr12:46009314-46009328

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:46009735-46009785	HUVEC	blood vessel:	n/a
2	chr12:46009735-46009785	A549	lung:	n/a
3	chr12:46009735-46009785	HRPEpiC	eye:	n/a
4	chr12:46009735-46009785	GM06990	blood:	n/a
5	chr12:46009735-46009785	MCF10A-Er-Src	breast:	n/a
6	chr12:46009735-46009785	HMEC	breast:	n/a
7	chr12:46009735-46009785	U87	brain:	n/a
8	chr12:46009735-46009785	ovcar-3	ovarian:	n/a
9	chr12:46009735-46009785	H1-hESC	embryonic stem cell:	embryo
10	chr12:46009735-46009785	GM19239	blood:	n/a
11	chr12:46009735-46009785	SKMC	muscle:	n/a
12	chr12:46009735-46009785	SK-N-SH	brain:	n/a
13	chr12:46009735-46009785	HL-60	blood:	n/a
14	chr12:46009735-46009785	LNCaP	prostate:	n/a
15	chr12:46009735-46009785	AG04450	lung:	fetal
16	chr12:46009735-46009785	SK-N-MC	brain:	n/a
17	chr12:46009735-46009785	ECC-1	luminal epithelium:	n/a
18	chr12:46009735-46009785	PrEC	prostate:	n/a
19	chr12:46009735-46009785	BE2_C	brain:	n/a
20	chr12:46009735-46009785	SAEC	small airway:	n/a
21	chr12:46009735-46009785	GM12878	blood:	n/a
22	chr12:46009735-46009785	PANC-1	pancreas:	n/a
23	chr12:46009735-46009785	CMK	blood:	n/a
24	chr12:46009735-46009785	T-47D	breast:	n/a
25	chr12:46009735-46009785	AG10803	skin:	n/a
26	chr12:46009735-46009785	HepG2	liver:	n/a
27	chr12:46009735-46009785	Jurkat	blood:	n/a
28	chr12:46009735-46009785	Caco-2	colon:	n/a
29	chr12:46009735-46009785	HCT-116	colon:	n/a
30	chr12:46009735-46009785	HRE	kidney:	n/a
31	chr12:46009735-46009785	NT2-D1	testis:	n/a
32	chr12:46009735-46009785	SK-N-SH_RA	brain:	n/a
33	chr12:46009735-46009785	NHDF-neo	bronchial:	n/a
34	chr12:46009735-46009785	AoSMC	blood vessel:	n/a
35	chr12:46009735-46009785	HEEpiC	esophagus:	n/a
36	chr12:46009735-46009785	GM12891	blood:	n/a
37	chr12:46009735-46009785	Hela-S3	cervix:	n/a
38	chr12:46009735-46009785	HIPEpiC	eye:	n/a
39	chr12:46009735-46009785	NB4	blood:	n/a
40	chr12:46009735-46009785	HPAEpiC	pulmonary alveolar:	n/a
41	chr12:46009735-46009785	RPTEC	kidney:	n/a
42	chr12:46009735-46009785	Hepatocyte	liver:	n/a
43	chr12:46009735-46009785	ProgFib	skin:	n/a
44	chr12:46009735-46009785	MCF-7	breast:	n/a
45	chr12:46009735-46009785	AG04449	skin:	fetal
46	chr12:46009735-46009785	HCF	heart:	n/a
47	chr12:46009735-46009785	NHBE	bronchial:	n/a
48	chr12:46009735-46009785	HAEpiC	amniotic membrane:	n/a
49	chr12:46009735-46009785	GM12892	blood:	n/a
50	chr12:46009735-46009785	HCPEpiC	choroid plexus:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:46000607..46002372-chr12:46007311..46008913,2	MCF-7	breast:
2	chr12:46003941..46007614-chr12:46011216..46015069,3	K562	blood:
3	chr12:45989699..45991915-chr12:46007034..46009721,2	MCF-7	breast:
4	chr12:46014914..46017037-chr12:46380285..46382180,2	MCF-7	breast:
5	chr12:46009974..46011818-chr12:46122972..46124815,2	K562	blood:
6	chr12:46011580..46014039-chr12:46017098..46019147,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000257657	TF binding region
ENSG00000257657	CpG island
ENSG00000189079	chromatin interactions
ENSG00000257657	chromatin interactions

Extended variants
information (count: 238 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:238 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs35901207	chr12:46008684-46008685	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs190310438	chr12:46008699-46008700	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs530084428	chr12:46008735-46008736	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs182876676	chr12:46008740-46008741	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs139947868	chr12:46008752-46008753	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs75831205	chr12:46008763-46008764	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs187511404	chr12:46008816-46008817	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs539180411	chr12:46008823-46008824	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs147234602	chr12:46008875-46008876	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs575720852	chr12:46008937-46008938	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs12578402	chr12:46008948-46008949	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs554873144	chr12:46008954-46008955	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs58099600	chr12:46008991-46008992	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs540506203	chr12:46009009-46009010	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs570649078	chr12:46009104-46009105	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs564961632	chr12:46009122-46009123	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs57938779	chr12:46009229-46009230	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs543944162	chr12:46009323-46009324	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs193072103	chr12:46009349-46009350	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs184164700	chr12:46009414-46009415	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs118182039	chr12:46009466-46009467	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs547841058	chr12:46009481-46009482	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs35910505	chr12:46009485-46009486	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs560077856	chr12:46009499-46009500	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs148715512	chr12:46009510-46009511	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs2712590	chr12:46009521-46009522	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs147142957	chr12:46009541-46009542	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs200308184	chr12:46009543-46009544	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs187514196	chr12:46009544-46009545	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs539197056	chr12:46009562-46009563	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs192749033	chr12:46009564-46009565	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs142299287	chr12:46009657-46009658	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs536662102	chr12:46009678-46009679	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs554700412	chr12:46009723-46009724	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs151320974	chr12:46009735-46009736	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs34059504	chr12:46009841-46009842	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs78950496	chr12:46009842-46009843	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs558805606	chr12:46009853-46009854	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs184012453	chr12:46009854-46009855	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs140639142	chr12:46009894-46009895	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs112120103	chr12:46009910-46009911	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs188697149	chr12:46009941-46009942	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs58817739	chr12:46009960-46009961	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs2712591	chr12:46009971-46009972	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs559937846	chr12:46009975-46009976	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs144370833	chr12:46010000-46010001	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs146607415	chr12:46010005-46010006	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs532043923	chr12:46010051-46010052	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs140264788	chr12:46010140-46010141	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs60079481	chr12:46010230-46010231	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:63)

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
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
Hirschsprung''s Disease	21712996	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	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
low-grade B-cell lymphoma tumor	18367492	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
Gastric cancer	18160780	CNVD
Myelofibrosis	22110671	CNVD
Follicular lymphoma	20505157	CNVD
Hepatocellular carcinoma	16750200	CNVD
Melanoma	18172304	CNVD
Metanephric adenoma	20802469	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Bladder cancer	21909424	CNVD

Chromatin state (count:64 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:46005400-46009000	Weak transcription	NH-A	brain
2	chr12:46005400-46009400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr12:46005400-46009400	Weak transcription	NHEK	skin
4	chr12:46005400-46011800	Weak transcription	Right Atrium	heart
5	chr12:46005600-46009200	Weak transcription	Brain Inferior Temporal Lobe	brain
6	chr12:46006200-46009000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr12:46006200-46009000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr12:46006200-46009000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr12:46006400-46009000	Weak transcription	Osteobl	bone
10	chr12:46006400-46009200	Weak transcription	NHDF-Ad	bronchial
11	chr12:46007000-46009000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr12:46007200-46009800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr12:46007600-46009200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr12:46007600-46009200	Weak transcription	Brain Cingulate Gyrus	brain
15	chr12:46007600-46009600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr12:46007600-46010600	Enhancers	Hela-S3	cervix
17	chr12:46008000-46008800	Weak transcription	NHLF	lung
18	chr12:46008000-46009000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr12:46008200-46009600	Weak transcription	Colon Smooth Muscle	Colon
20	chr12:46008200-46009800	Enhancers	Brain Anterior Caudate	brain
21	chr12:46008400-46009000	Weak transcription	Brain Hippocampus Middle	brain
22	chr12:46008600-46010000	Enhancers	Muscle Satellite Cultured Cells	--
23	chr12:46008600-46010000	Enhancers	HUVEC	blood vessel
24	chr12:46008800-46009800	Enhancers	A549	lung
25	chr12:46008800-46010200	Enhancers	NHLF	lung
26	chr12:46009000-46009600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr12:46009000-46009800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr12:46009000-46009800	Enhancers	Brain Hippocampus Middle	brain
29	chr12:46009000-46009800	Enhancers	Skeletal Muscle Male	skeletal muscle
30	chr12:46009000-46009800	Enhancers	HSMM	muscle
31	chr12:46009000-46009800	Enhancers	NH-A	brain
32	chr12:46009000-46009800	Enhancers	Osteobl	bone
33	chr12:46009000-46010000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr12:46009000-46010000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr12:46009000-46010000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr12:46009000-46010000	Enhancers	Fetal Kidney	kidney
37	chr12:46009000-46010000	Enhancers	HSMMtube	muscle
38	chr12:46009200-46009400	Enhancers	Brain Cingulate Gyrus	brain
39	chr12:46009200-46009600	Enhancers	Primary hematopoietic stem cells short term culture	blood
40	chr12:46009200-46009600	Enhancers	Brain Angular Gyrus	brain
41	chr12:46009200-46009600	Enhancers	Brain Inferior Temporal Lobe	brain
42	chr12:46009200-46009800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr12:46009200-46009800	Enhancers	Psoas Muscle	Psoas
44	chr12:46009200-46010000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr12:46009200-46010000	Enhancers	HMEC	breast
46	chr12:46009200-46010000	Enhancers	NHDF-Ad	bronchial
47	chr12:46009400-46009800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr12:46009400-46009800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr12:46009400-46009800	Flanking Active TSS	Brain Cingulate Gyrus	brain
50	chr12:46009400-46009800	Enhancers	NHEK	skin

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