Variant report

Variant	nsv899310
Chromosome Location	chr12:75682796-75707396
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:152)
CpG islands
(count:611)
Chromatin interactive
region (count:17)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:152 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:75684118-75684145	HepG2	liver:	n/a	n/a
2	BHLHE40	chr12:75705326-75705478	GM12878	blood:	n/a	n/a
3	BHLHE40	chr12:75705424-75705607	K562	blood:	n/a	n/a
4	BHLHE40	chr12:75705337-75705530	HepG2	liver:	n/a	n/a
5	CEBPB	chr12:75702100-75702456	IMR90	lung:	n/a	chr12:75702269-75702280
6	CEBPB	chr12:75684823-75685090	A549	lung:	n/a	chr12:75684985-75684996
7	CEBPB	chr12:75684893-75685084	HepG2	liver:	n/a	chr12:75684985-75684996
8	CEBPB	chr12:75702265-75702453	H1-hESC	embryonic stem cell:	n/a	chr12:75702269-75702280
9	CEBPB	chr12:75684802-75685162	HepG2	liver:	n/a	chr12:75684985-75684996
10	CEBPB	chr12:75702088-75702433	HepG2	liver:	n/a	chr12:75702269-75702280
11	CEBPB	chr12:75702097-75702427	A549	lung:	n/a	chr12:75702269-75702280
12	CTCF	chr12:75683720-75683870	HRPEpiC	eye:	n/a	n/a
13	CTCF	chr12:75683720-75683870	RPTEC	kidney:	n/a	n/a
14	CTCF	chr12:75683660-75683810	HCPEpiC	choroid plexus:	n/a	n/a
15	CTCF	chr12:75683740-75683890	NHEK	skin:	n/a	n/a
16	CTCF	chr12:75683720-75683870	HVMF	connective:	n/a	n/a
17	CTCF	chr12:75683580-75683730	RPTEC	kidney:	n/a	n/a
18	CTCF	chr12:75683740-75683890	SAEC	small airway:	n/a	n/a
19	CTCF	chr12:75683700-75683850	HRPEpiC	eye:	n/a	n/a
20	CTCF	chr12:75683452-75683952	HCT-116	colon:	n/a	n/a
21	CTCF	chr12:75683680-75683830	HPAF	blood vessel:	n/a	n/a
22	CTCF	chr12:75683627-75683853	A549	lung:	n/a	n/a
23	CTCF	chr12:75683730-75683806	MCF-7	breast:	n/a	n/a
24	CTCF	chr12:75683713-75683836	GM12878	blood:	n/a	n/a
25	CTCF	chr12:75683741-75683841	GM10266	blood:	n/a	n/a
26	CTCF	chr12:75683700-75683850	AG04450	lung:	n/a	n/a
27	CTCF	chr12:75683740-75683890	AG09309	skin:	n/a	n/a
28	CTCF	chr12:75683620-75683770	HEEpiC	esophagus:	n/a	n/a
29	CTCF	chr12:75683649-75683878	ECC-1	luminal epithelium:	n/a	n/a
30	CTCF	chr12:75683720-75683870	AG09319	gingival:	n/a	n/a
31	CTCF	chr12:75683560-75684041	HCT-116	colon:	n/a	n/a
32	CTCF	chr12:75683740-75683890	WI-38	lung:	n/a	n/a
33	CTCF	chr12:75683700-75683850	AoAF	blood vessel:	n/a	n/a
34	CTCF	chr12:75683700-75683850	HA-sp	spinal cord:	n/a	n/a
35	CTCF	chr12:75683700-75683850	HFF-Myc	foreskin:	n/a	n/a
36	CTCF	chr12:75683550-75683908	MCF-7	breast:	n/a	n/a
37	CTCF	chr12:75683700-75683850	HCFaa	heart:	n/a	n/a
38	CTCF	chr12:75683780-75683930	HCT-116	colon:	n/a	n/a
39	CTCF	chr12:75683555-75683952	IMR90	lung:	n/a	n/a
40	CTCF	chr12:75683660-75683810	GM12878	blood:	n/a	n/a
41	CTCF	chr12:75683636-75684061	MCF-7	breast:	n/a	n/a
42	CTCF	chr12:75683618-75683830	ECC-1	luminal epithelium:	n/a	n/a
43	CTCF	chr12:75683680-75683830	NHDF-neo	bronchial:	n/a	n/a
44	CTCF	chr12:75683607-75683960	GM12878	blood:	n/a	n/a
45	CTCF	chr12:75683700-75683850	HPF	lung:	n/a	n/a
46	CTCF	chr12:75683548-75683992	A549	lung:	n/a	n/a
47	CTCF	chr12:75705481-75705558	K562	blood:	n/a	n/a
48	CTCF	chr12:75683680-75683830	HA-sp	spinal cord:	n/a	n/a
49	CTCF	chr12:75683680-75683830	HCPEpiC	choroid plexus:	n/a	n/a
50	CTCF	chr12:75683679-75683864	LNCaP	prostate:	n/a	n/a

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:75699625-75699675	IMR90	lung:	fetal
2	chr12:75699625-75699675	IMR90	lung:	fetal
3	chr12:75699252-75699302	HAEpiC	amniotic membrane:	n/a
4	chr12:75699311-75699361	U87	brain:	n/a
5	chr12:75707098-75707148	A549	lung:	n/a
6	chr12:75699992-75700042	SKMC	muscle:	n/a
7	chr12:75699992-75700042	HMEC	breast:	n/a
8	chr12:75699417-75699467	AG09319	gingival:	n/a
9	chr12:75703120-75703170	NHDF-neo	bronchial:	n/a
10	chr12:75699252-75699302	HIPEpiC	eye:	n/a
11	chr12:75699417-75699467	NB4	blood:	n/a
12	chr12:75699992-75700042	HCF	heart:	n/a
13	chr12:75699992-75700042	GM19239	blood:	n/a
14	chr12:75699311-75699361	SAEC	small airway:	n/a
15	chr12:75699311-75699361	HRPEpiC	eye:	n/a
16	chr12:75699512-75699562	HepG2	liver:	n/a
17	chr12:75699625-75699675	Jurkat	blood:	n/a
18	chr12:75699992-75700042	RPTEC	kidney:	n/a
19	chr12:75703120-75703170	RPTEC	kidney:	n/a
20	chr12:75703120-75703170	HRE	kidney:	n/a
21	chr12:75707098-75707148	Hela-S3	cervix:	n/a
22	chr12:75699252-75699302	HCPEpiC	choroid plexus:	n/a
23	chr12:75703120-75703170	HCT-116	colon:	n/a
24	chr12:75699417-75699467	MCF-7	breast:	n/a
25	chr12:75699417-75699467	HepG2	liver:	n/a
26	chr12:75699992-75700042	HCT-116	colon:	n/a
27	chr12:75699311-75699361	PANC-1	pancreas:	n/a
28	chr12:75699625-75699675	Hepatocyte	liver:	n/a
29	chr12:75703120-75703170	K562	blood:	n/a
30	chr12:75707098-75707148	HEEpiC	esophagus:	n/a
31	chr12:75707098-75707148	HCM	heart:	n/a
32	chr12:75699311-75699361	RPTEC	kidney:	n/a
33	chr12:75707098-75707148	GM12892	blood:	n/a
34	chr12:75699252-75699302	Hela-S3	cervix:	n/a
35	chr12:75699992-75700042	HRPEpiC	eye:	n/a
36	chr12:75699625-75699675	Hela-S3	cervix:	n/a
37	chr12:75703120-75703170	Caco-2	colon:	n/a
38	chr12:75699311-75699361	HCT-116	colon:	n/a
39	chr12:75697264-75697314	HIPEpiC	eye:	n/a
40	chr12:75707098-75707148	NHDF-neo	bronchial:	n/a
41	chr12:75699625-75699675	K562	blood:	n/a
42	chr12:75697264-75697314	T-47D	breast:	n/a
43	chr12:75699512-75699562	Hela-S3	cervix:	n/a
44	chr12:75707098-75707148	LNCaP	prostate:	n/a
45	chr12:75699311-75699361	PrEC	prostate:	n/a
46	chr12:75699512-75699562	HRE	kidney:	n/a
47	chr12:75699625-75699675	PrEC	prostate:	n/a
48	chr12:75699992-75700042	HEEpiC	esophagus:	n/a
49	chr12:75699311-75699361	HPAEpiC	pulmonary alveolar:	n/a
50	chr12:75699512-75699562	AG04449	skin:	fetal

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:75691783..75694692-chr12:75701751..75704266,2	MCF-7	breast:
2	chr12:75694427..75696955-chr12:75721959..75724062,2	MCF-7	breast:
3	chr12:75140866..75141740-chr12:75683619..75684268,4	MCF-7	breast:
4	chr12:75143585..75146196-chr12:75682282..75684719,2	MCF-7	breast:
5	chr12:75698920..75700864-chr12:75702519..75704425,2	MCF-7	breast:
6	chr12:75691783..75694692-chr12:75701751..75704266,2	MCF-7	breast:
7	chr12:75692083..75694808-chr12:75698140..75700535,3	MCF-7	breast:
8	chr12:75706260..75708940-chr12:75711977..75713513,2	MCF-7	breast:
9	chr12:75265370..75266267-chr12:75683003..75683605,2	MCF-7	breast:
10	chr12:75628651..75631395-chr12:75681833..75683806,2	MCF-7	breast:
11	chr12:75552568..75553111-chr12:75683666..75684233,2	MCF-7	breast:
12	chr12:75665105..75667577-chr12:75682796..75684340,2	MCF-7	breast:
13	chr12:75675181..75678021-chr12:75682376..75684656,2	MCF-7	breast:
14	chr12:75701954..75704908-chr12:75713471..75715779,3	MCF-7	breast:
15	chr12:75548709..75551411-chr12:75681695..75683989,2	MCF-7	breast:
16	chr12:75563611..75565633-chr12:75680555..75683194,2	MCF-7	breast:
17	chr12:75265352..75266271-chr12:75682822..75683455,2	MCF-7	breast:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GLIPR1L1-1	chr12:75688823-75688892	ENSG00000254451.2
2	lnc-GLIPR1L1-1	chr12:75688836-75688948	ENSG00000254451.2
3	lnc-GLIPR1L1-1	chr12:75691980-75692288	ENSG00000254451.2

No data

Variant related genes	Relation type
ENSG00000254451	TF binding region
ENSG00000257823	TF binding region
ENSG00000254451	CpG island
ENSG00000257823	CpG island
ENSG00000257823	chromatin interactions
ENSG00000180881	chromatin interactions
ENSG00000254451	chromatin interactions

Extended variants
information (count: 959 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:959 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3924594	chr12:75682796-75682797	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs555442826	chr12:75682820-75682821	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs370420182	chr12:75682838-75682839	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs376414242	chr12:75682843-75682844	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs111617312	chr12:75682871-75682872	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs113032674	chr12:75682904-75682905	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs140536831	chr12:75682925-75682926	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs375351950	chr12:75682932-75682933	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs145615398	chr12:75682947-75682948	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs138331268	chr12:75682964-75682965	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs77060435	chr12:75682970-75682971	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs11180445	chr12:75683014-75683015	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs143157334	chr12:75683052-75683053	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs148241216	chr12:75683064-75683065	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs191094366	chr12:75683148-75683149	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs527455782	chr12:75683189-75683190	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs540856415	chr12:75683202-75683203	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs564024977	chr12:75683221-75683222	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs535735436	chr12:75683240-75683241	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs533115090	chr12:75683267-75683268	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs182933190	chr12:75683327-75683328	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs375986205	chr12:75683357-75683358	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs112805358	chr12:75683412-75683413	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs370428667	chr12:75683427-75683428	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs201840767	chr12:75683456-75683457	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs139225720	chr12:75683457-75683458	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs367762993	chr12:75683463-75683464	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs548767303	chr12:75683497-75683498	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs367774244	chr12:75683505-75683506	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs199654216	chr12:75683519-75683520	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs144198119	chr12:75683520-75683521	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs146549801	chr12:75683533-75683534	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs113629658	chr12:75683546-75683547	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs191110069	chr12:75683583-75683584	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs111709227	chr12:75683597-75683598	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs539039943	chr12:75683609-75683610	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs571969398	chr12:75683614-75683615	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs149880273	chr12:75683616-75683617	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs555876843	chr12:75683633-75683634	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs183422645	chr12:75683638-75683639	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs573920293	chr12:75683657-75683658	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs555686849	chr12:75683674-75683675	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs543030476	chr12:75683724-75683725	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs553028978	chr12:75683726-75683727	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs573037660	chr12:75683745-75683746	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs540817996	chr12:75683746-75683747	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs141380318	chr12:75683767-75683768	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs188001979	chr12:75683780-75683781	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs563614647	chr12:75683862-75683863	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs575713838	chr12:75683874-75683875	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:73)

Disease	PMID	Source
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
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
Neurodevelopmental disorder	22521361	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
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Burkitt''s lymphoma	20823134	CNVD
abnormal development	18461090	CNVD
Prostate cancer	18632612	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
craniofacial dysmorphism	21918468	CNVD
Breast cancer	17133270	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	22032731	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
Hodgkin''s lymphoma	18641027	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Urothelial cell carcinoma	18451213	CNVD
Myelofibrosis	22110671	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:90 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:75679600-75699200	Weak transcription	Aorta	Aorta
2	chr12:75680800-75682800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr12:75681200-75711400	Weak transcription	Psoas Muscle	Psoas
4	chr12:75682200-75691800	Weak transcription	Ovary	ovary
5	chr12:75682200-75699200	Weak transcription	Right Ventricle	heart
6	chr12:75682600-75699200	Weak transcription	Left Ventricle	heart
7	chr12:75682800-75683400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
8	chr12:75683400-75697200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
9	chr12:75684600-75685000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr12:75687800-75688600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
11	chr12:75687800-75689200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
12	chr12:75688200-75688400	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr12:75688200-75688400	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr12:75688200-75689200	Enhancers	H1 Cell Line	embryonic stem cell
15	chr12:75688200-75689400	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr12:75688200-75689400	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr12:75688200-75689400	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr12:75688400-75688800	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
19	chr12:75688400-75689000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
20	chr12:75688600-75688800	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr12:75688800-75689200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
22	chr12:75688800-75689400	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr12:75689000-75689200	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr12:75689800-75697200	Weak transcription	Adipose Nuclei	Adipose
25	chr12:75690200-75699400	Weak transcription	Stomach Smooth Muscle	stomach
26	chr12:75690600-75697200	Weak transcription	Brain Hippocampus Middle	brain
27	chr12:75691000-75699600	Weak transcription	Duodenum Smooth Muscle	Duodenum
28	chr12:75691400-75691800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr12:75691600-75697200	Weak transcription	Brain Anterior Caudate	brain
30	chr12:75691800-75692400	Strong transcription	Ovary	ovary
31	chr12:75691800-75699400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr12:75692400-75699200	Weak transcription	Ovary	ovary
33	chr12:75694600-75695200	Enhancers	Liver	Liver
34	chr12:75695000-75696800	Weak transcription	Skeletal Muscle Female	skeletal muscle
35	chr12:75695200-75697600	Weak transcription	Liver	Liver
36	chr12:75695400-75699200	Weak transcription	Pancreas	Pancrea
37	chr12:75695800-75696200	Enhancers	Fetal Brain Female	brain
38	chr12:75696000-75706000	Weak transcription	Skeletal Muscle Male	skeletal muscle
39	chr12:75696200-75698800	Weak transcription	Brain Inferior Temporal Lobe	brain
40	chr12:75696200-75699200	Weak transcription	Lung	lung
41	chr12:75696200-75706000	Weak transcription	Esophagus	oesophagus
42	chr12:75696400-75706800	Weak transcription	Brain Angular Gyrus	brain
43	chr12:75696600-75701600	Weak transcription	Brain Cingulate Gyrus	brain
44	chr12:75696800-75697000	Strong transcription	Skeletal Muscle Female	skeletal muscle
45	chr12:75697000-75707400	Weak transcription	Skeletal Muscle Female	skeletal muscle
46	chr12:75697200-75697800	Strong transcription	Brain Anterior Caudate	brain
47	chr12:75697200-75698000	Strong transcription	Brain Hippocampus Middle	brain
48	chr12:75697200-75698200	Strong transcription	Adipose Nuclei	Adipose
49	chr12:75697200-75700000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
50	chr12:75697200-75700000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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