Variant report

Variant	esv1799099
Chromosome Location	chr12:122382229-122398494
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	BACH1	chr12:122387829-122387915	K562	blood:	n/a	n/a
2	BHLHE40	chr12:122387953-122388292	HepG2	liver:	n/a	n/a
3	BHLHE40	chr12:122388007-122388191	A549	lung:	n/a	n/a
4	CBX3	chr12:122384296-122384525	K562	blood:	n/a	n/a
5	CBX3	chr12:122384169-122384621	K562	blood:	n/a	n/a
6	CEBPB	chr12:122387919-122388342	IMR90	lung:	n/a	n/a
7	CEBPB	chr12:122394416-122394504	K562	blood:	n/a	n/a
8	CEBPB	chr12:122396757-122397055	IMR90	lung:	n/a	n/a
9	CEBPB	chr12:122394419-122394499	IMR90	lung:	n/a	n/a
10	CTCF	chr12:122393740-122393890	HMEC	breast:	n/a	chr12:122393845-122393858 chr12:122393842-122393860
11	CTCF	chr12:122393760-122393910	Caco-2	colon:	n/a	chr12:122393845-122393858 chr12:122393842-122393860
12	CTCF	chr12:122393801-122393916	GM20000	blood:	n/a	chr12:122393845-122393858 chr12:122393842-122393860
13	CTCF	chr12:122393728-122393953	A549	lung:	n/a	chr12:122393845-122393858 chr12:122393842-122393860
14	CTCF	chr12:122393691-122393954	HepG2	liver:	n/a	chr12:122393845-122393858 chr12:122393842-122393860
15	CTCF	chr12:122393800-122393950	GM12870	blood:	n/a	chr12:122393845-122393858 chr12:122393842-122393860
16	CTCF	chr12:122393800-122393950	WERI-Rb-1	eye:	n/a	chr12:122393845-122393858 chr12:122393842-122393860
17	CTCF	chr12:122393780-122393930	HVMF	connective:	n/a	chr12:122393845-122393858 chr12:122393842-122393860
18	CTCF	chr12:122393820-122393970	GM06990	blood:	n/a	chr12:122393845-122393858 chr12:122393842-122393860
19	CTCF	chr12:122389640-122389696	GM13976	blood:	n/a	n/a
20	CTCF	chr12:122394020-122394170	NHEK	skin:	n/a	n/a
21	CTCF	chr12:122393800-122393950	HCFaa	heart:	n/a	chr12:122393845-122393858 chr12:122393842-122393860
22	CTCF	chr12:122393774-122393922	GM12892	blood:	n/a	chr12:122393845-122393858 chr12:122393842-122393860
23	CTCF	chr12:122393820-122393970	GM12864	blood:	n/a	chr12:122393845-122393858 chr12:122393842-122393860
24	CTCF	chr12:122393759-122393958	Medullo	brain:	n/a	chr12:122393845-122393858 chr12:122393842-122393860
25	CTCF	chr12:122393340-122394155	A549	lung:	n/a	chr12:122393845-122393858 chr12:122393842-122393860
26	CTCF	chr12:122393820-122393970	K562	blood:	n/a	chr12:122393845-122393858 chr12:122393842-122393860
27	CTCF	chr12:122393780-122393930	SK-N-SH_RA	brain:	n/a	chr12:122393845-122393858 chr12:122393842-122393860
28	CTCF	chr12:122393800-122393950	HUVEC	blood vessel:	n/a	chr12:122393845-122393858 chr12:122393842-122393860
29	CTCF	chr12:122393756-122393921	MCF-7	breast:	n/a	chr12:122393845-122393858 chr12:122393842-122393860
30	CTCF	chr12:122393741-122393919	Lung_OC	lung:	n/a	chr12:122393845-122393858 chr12:122393842-122393860
31	CTCF	chr12:122393760-122393910	AG09309	skin:	n/a	chr12:122393845-122393858 chr12:122393842-122393860
32	CTCF	chr12:122393760-122393910	GM12874	blood:	n/a	chr12:122393845-122393858 chr12:122393842-122393860
33	CTCF	chr12:122393737-122393955	GM12878	blood:	n/a	chr12:122393845-122393858 chr12:122393842-122393860
34	CTCF	chr12:122393860-122394010	NHEK	skin:	n/a	n/a
35	CTCF	chr12:122393760-122393910	GM12873	blood:	n/a	chr12:122393845-122393858 chr12:122393842-122393860
36	CTCF	chr12:122393780-122393930	AG04449	skin:	n/a	chr12:122393845-122393858 chr12:122393842-122393860
37	CTCF	chr12:122393820-122393970	AG10803	skin:	n/a	chr12:122393845-122393858 chr12:122393842-122393860
38	CTCF	chr12:122393730-122393962	K562	blood:	n/a	chr12:122393845-122393858 chr12:122393842-122393860
39	CTCF	chr12:122393820-122393970	NHDF-neo	bronchial:	n/a	chr12:122393845-122393858 chr12:122393842-122393860
40	CTCF	chr12:122393759-122394007	A549	lung:	n/a	chr12:122393845-122393858 chr12:122393842-122393860
41	CTCF	chr12:122393740-122393890	HRPEpiC	eye:	n/a	chr12:122393845-122393858 chr12:122393842-122393860
42	CTCF	chr12:122393650-122393984	K562	blood:	n/a	chr12:122393845-122393858 chr12:122393842-122393860
43	CTCF	chr12:122393749-122393947	LNCaP	prostate:	n/a	chr12:122393845-122393858 chr12:122393842-122393860
44	CTCF	chr12:122393780-122393930	GM12871	blood:	n/a	chr12:122393845-122393858 chr12:122393842-122393860
45	CTCF	chr12:122393740-122393890	HCM	heart:	n/a	chr12:122393845-122393858 chr12:122393842-122393860
46	CTCF	chr12:122393616-122394076	MCF-7	breast:	n/a	chr12:122393845-122393858 chr12:122393842-122393860
47	CTCF	chr12:122393780-122393930	AG09319	gingival:	n/a	chr12:122393845-122393858 chr12:122393842-122393860
48	CTCF	chr12:122393760-122393910	K562	blood:	n/a	chr12:122393845-122393858 chr12:122393842-122393860
49	CTCF	chr12:122393750-122393932	GM10248	blood:	n/a	chr12:122393845-122393858 chr12:122393842-122393860
50	CTCF	chr12:122393800-122393950	GM12868	blood:	n/a	chr12:122393845-122393858 chr12:122393842-122393860

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:122396677-122396727	GM19239	blood:	n/a
2	chr12:122396677-122396727	U87	brain:	n/a
3	chr12:122386353-122386403	HEEpiC	esophagus:	n/a
4	chr12:122396677-122396727	ECC-1	luminal epithelium:	n/a
5	chr12:122396687-122396737	HUVEC	blood vessel:	n/a
6	chr12:122396687-122396737	HAEpiC	amniotic membrane:	n/a
7	chr12:122396633-122396683	SK-N-SH	brain:	n/a
8	chr12:122396633-122396683	MCF-7	breast:	n/a
9	chr12:122386353-122386403	ProgFib	skin:	n/a
10	chr12:122396687-122396737	NHDF-neo	bronchial:	n/a
11	chr12:122396677-122396727	GM06990	blood:	n/a
12	chr12:122396677-122396727	HMEC	breast:	n/a
13	chr12:122396633-122396683	SK-N-MC	brain:	n/a
14	chr12:122386353-122386403	HCT-116	colon:	n/a
15	chr12:122396633-122396683	K562	blood:	n/a
16	chr12:122396687-122396737	Hela-S3	cervix:	n/a
17	chr12:122396687-122396737	IMR90	lung:	fetal
18	chr12:122396677-122396727	HAEpiC	amniotic membrane:	n/a
19	chr12:122396633-122396683	NT2-D1	testis:	n/a
20	chr12:122396677-122396727	MCF10A-Er-Src	breast:	n/a
21	chr12:122396677-122396727	HCPEpiC	choroid plexus:	n/a
22	chr12:122396677-122396727	CMK	blood:	n/a
23	chr12:122396677-122396727	T-47D	breast:	n/a
24	chr12:122396687-122396737	HCF	heart:	n/a
25	chr12:122396687-122396737	GM06990	blood:	n/a
26	chr12:122396677-122396727	HL-60	blood:	n/a
27	chr12:122396633-122396683	IMR90	lung:	fetal
28	chr12:122396687-122396737	NHBE	bronchial:	n/a
29	chr12:122396687-122396737	NH-A	brain:	n/a
30	chr12:122396633-122396683	HCPEpiC	choroid plexus:	n/a
31	chr12:122386353-122386403	K562	blood:	n/a
32	chr12:122396677-122396727	AG04449	skin:	fetal
33	chr12:122396633-122396683	AG04450	lung:	fetal
34	chr12:122396677-122396727	HCT-116	colon:	n/a
35	chr12:122386353-122386403	SK-N-SH	brain:	n/a
36	chr12:122386353-122386403	HNPCEpiC	eye:	n/a
37	chr12:122396677-122396727	PANC-1	pancreas:	n/a
38	chr12:122396687-122396737	A549	lung:	n/a
39	chr12:122396687-122396737	RPTEC	kidney:	n/a
40	chr12:122396633-122396683	HRPEpiC	eye:	n/a
41	chr12:122396633-122396683	HepG2	liver:	n/a
42	chr12:122396633-122396683	H1-hESC	embryonic stem cell:	embryo
43	chr12:122396677-122396727	H1-hESC	embryonic stem cell:	embryo
44	chr12:122396633-122396683	HAEpiC	amniotic membrane:	n/a
45	chr12:122396687-122396737	ovcar-3	ovarian:	n/a
46	chr12:122386353-122386403	SK-N-SH_RA	brain:	n/a
47	chr12:122396687-122396737	AG04450	lung:	fetal
48	chr12:122396677-122396727	SAEC	small airway:	n/a
49	chr12:122396677-122396727	HRPEpiC	eye:	n/a
50	chr12:122396677-122396727	ovcar-3	ovarian:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:122393339..122394256-chr12:122469215..122470133,3	MCF-7	breast:
2	chr12:122394265..122395832-chr12:122468104..122470419,2	MCF-7	breast:
3	chr12:122367527..122369805-chr12:122380881..122383741,2	K562	blood:
4	chr12:122391317..122393774-chr12:122396959..122400583,3	K562	blood:
5	chr12:122393562..122396353-chr12:122460972..122463920,2	K562	blood:
6	chr12:122395836..122398173-chr12:122399346..122401443,3	MCF-7	breast:
7	chr12:122383104..122386002-chr12:122399746..122401502,2	K562	blood:
8	chr12:122325328..122328082-chr12:122382388..122384229,2	K562	blood:
9	chr12:122393647..122395648-chr12:122451452..122452969,2	MCF-7	breast:
10	chr12:122394100..122396317-chr12:122458404..122460674,2	MCF-7	breast:
11	chr12:122392019..122395422-chr12:122459047..122461618,4	MCF-7	breast:
12	chr12:122380214..122384084-chr12:122388242..122390688,3	K562	blood:
13	chr12:122393570..122396263-chr12:122456754..122459004,2	MCF-7	breast:
14	chr12:122394365..122397309-chr12:122398081..122400536,2	K562	blood:
15	chr12:122390662..122395297-chr12:122466472..122469968,4	MCF-7	breast:
16	chr12:122240547..122242267-chr12:122395940..122398933,2	K562	blood:
17	chr12:122377347..122378938-chr12:122380678..122382509,2	MCF-7	breast:
18	chr12:122385316..122388171-chr12:122391826..122394372,2	MCF-7	breast:
19	chr12:122393592..122395779-chr12:122400656..122403431,2	MCF-7	breast:
20	chr12:122391300..122395865-chr12:122397802..122402180,6	K562	blood:
21	chr12:122370436..122373370-chr12:122395690..122398094,3	K562	blood:
22	chr12:122392364..122395204-chr12:122467320..122469224,2	K562	blood:

Variant related genes	Relation type
WDR66	TF binding region
WDR66	CpG island
ENSG00000255856	chromatin interactions
ENSG00000158023	chromatin interactions
ENSG00000110801	chromatin interactions
ENSG00000212694	chromatin interactions
ENSG00000110987	chromatin interactions
ENSG00000139718	chromatin interactions
ENSG00000256950	chromatin interactions
ENSG00000139725	chromatin interactions

Extended variants
information (count: 634 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:634 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1720037	chr12:122382229-122382230	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs553100473	chr12:122382310-122382311	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs577439309	chr12:122382319-122382320	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs543326770	chr12:122382341-122382342	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs189654199	chr12:122382349-122382350	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs545055194	chr12:122382412-122382413	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs563453142	chr12:122382429-122382430	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs181233115	chr12:122382436-122382437	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs542610691	chr12:122382574-122382575	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs377538313	chr12:122382588-122382589	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs561154975	chr12:122382592-122382593	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs528766921	chr12:122382634-122382635	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs185824297	chr12:122382654-122382655	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs74538720	chr12:122382709-122382710	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs80146824	chr12:122382716-122382717	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs551234803	chr12:122382721-122382722	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs569763729	chr12:122382749-122382750	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs190541343	chr12:122382750-122382751	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs555324082	chr12:122382751-122382752	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs567168706	chr12:122382836-122382837	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs56304060	chr12:122382861-122382862	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs552997124	chr12:122382900-122382901	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs540941463	chr12:122382919-122382920	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs11043258	chr12:122382936-122382937	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs544796313	chr12:122382952-122382953	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs374043720	chr12:122382968-122382969	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs575313740	chr12:122382969-122382970	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs542789589	chr12:122383015-122383016	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs560365627	chr12:122383037-122383038	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs183103709	chr12:122383042-122383043	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs528479503	chr12:122383112-122383113	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs78268210	chr12:122383147-122383148	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs186319464	chr12:122383148-122383149	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs370816193	chr12:122383149-122383150	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs532901381	chr12:122383171-122383172	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs551170921	chr12:122383223-122383224	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs569503975	chr12:122383233-122383234	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs71917340	chr12:122383234-122383235	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs11043259	chr12:122383238-122383239	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs60195039	chr12:122383243-122383244	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs531991501	chr12:122383248-122383249	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs12825811	chr12:122383258-122383259	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs534333581	chr12:122383263-122383264	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs546616822	chr12:122383271-122383272	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs571206393	chr12:122383286-122383287	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs538576011	chr12:122383291-122383292	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs556722973	chr12:122383313-122383314	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs191070579	chr12:122383318-122383319	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs536703637	chr12:122383364-122383365	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs554773971	chr12:122383387-122383388	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:73)

Disease	PMID	Source
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
Chronic lymphocytic leukemia	21546498	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	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
T-cell prolymphocytic leukemia	19278963	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
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Cancer	16751803	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Wilms tumour	21544195	CNVD
Ovarian cancer	21720365	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	16397240	CNVD
Breast cancer	17133270	CNVD
Breast cancer	17603634	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Cryptorchidism	21048976	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Neuroblastoma	18923191	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21806811	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Beckwith-Wiedemann syndrome	20648245	CNVD
Developmental delay	21457577	CNVD
dysmorphic	21457577	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chordoma	18071362	CNVD
Breast cancer	21509527	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:316 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:122357000-122383600	Weak transcription	Primary T cells from cord blood	blood
2	chr12:122363000-122384800	Weak transcription	Psoas Muscle	Psoas
3	chr12:122363000-122393400	Weak transcription	Brain Angular Gyrus	brain
4	chr12:122363200-122384600	Weak transcription	Brain Cingulate Gyrus	brain
5	chr12:122363600-122383600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr12:122363600-122383800	Weak transcription	Fetal Brain Male	brain
7	chr12:122363600-122385600	Weak transcription	Fetal Lung	lung
8	chr12:122363600-122392200	Weak transcription	Left Ventricle	heart
9	chr12:122363600-122398600	Weak transcription	Skeletal Muscle Male	skeletal muscle
10	chr12:122363600-122408000	Weak transcription	Right Ventricle	heart
11	chr12:122365600-122385800	Weak transcription	Fetal Muscle Trunk	muscle
12	chr12:122365600-122393400	Weak transcription	Brain Substantia Nigra	brain
13	chr12:122365800-122390200	Weak transcription	HUVEC	blood vessel
14	chr12:122365800-122405000	Weak transcription	Placenta Amnion	Placenta Amnion
15	chr12:122370600-122387800	Weak transcription	NHDF-Ad	bronchial
16	chr12:122370600-122403200	Weak transcription	Fetal Kidney	kidney
17	chr12:122372200-122396400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr12:122372800-122393600	Weak transcription	Brain Hippocampus Middle	brain
19	chr12:122374000-122402800	Weak transcription	HSMM	muscle
20	chr12:122374000-122405600	Weak transcription	Adipose Nuclei	Adipose
21	chr12:122375400-122401400	Weak transcription	Ovary	ovary
22	chr12:122375400-122402600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr12:122375600-122384000	Weak transcription	A549	lung
24	chr12:122375800-122384000	Weak transcription	Cortex derived primary cultured neurospheres	brain
25	chr12:122375800-122385800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr12:122375800-122393600	Weak transcription	Brain Inferior Temporal Lobe	brain
27	chr12:122375800-122415800	Weak transcription	Liver	Liver
28	chr12:122376000-122388000	Weak transcription	NHLF	lung
29	chr12:122376000-122393400	Weak transcription	Brain Anterior Caudate	brain
30	chr12:122376000-122401600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
31	chr12:122376000-122413000	Weak transcription	Aorta	Aorta
32	chr12:122377400-122383200	Weak transcription	Fetal Intestine Small	intestine
33	chr12:122377400-122406200	Weak transcription	Thymus	Thymus
34	chr12:122378600-122384400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr12:122378800-122384200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr12:122379400-122383200	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr12:122379800-122382400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr12:122380200-122383000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr12:122380600-122384400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr12:122380600-122387800	Weak transcription	Muscle Satellite Cultured Cells	--
41	chr12:122380600-122401600	Weak transcription	Pancreas	Pancrea
42	chr12:122380800-122384000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
43	chr12:122380800-122384400	Weak transcription	Fetal Thymus	thymus
44	chr12:122380800-122385600	Weak transcription	NH-A	brain
45	chr12:122380800-122387200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr12:122380800-122405800	Weak transcription	Skeletal Muscle Female	skeletal muscle
47	chr12:122381000-122382600	Strong transcription	Osteobl	bone
48	chr12:122381000-122384000	Weak transcription	Gastric	stomach
49	chr12:122381000-122384400	Weak transcription	Fetal Stomach	stomach
50	chr12:122381000-122387400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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