Variant report

Variant	nsv1042967
Chromosome Location	chr12:40629636-40710319
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	ARID3A	chr12:40681210-40681513	HepG2	liver:	n/a	n/a
2	ATF2	chr12:40707693-40708075	GM12878	blood:	n/a	n/a
3	ATF2	chr12:40656402-40656862	GM12878	blood:	n/a	n/a
4	ATF2	chr12:40707639-40708167	GM12878	blood:	n/a	n/a
5	ATF2	chr12:40656311-40656835	GM12878	blood:	n/a	n/a
6	ATF2	chr12:40655686-40656207	GM12878	blood:	n/a	n/a
7	ATF2	chr12:40655786-40656165	GM12878	blood:	n/a	n/a
8	ATF3	chr12:40680957-40681637	A549	lung:	n/a	n/a
9	ATF3	chr12:40680924-40681633	A549	lung:	n/a	n/a
10	BATF	chr12:40656446-40656805	GM12878	blood:	n/a	n/a
11	BATF	chr12:40707717-40708130	GM12878	blood:	n/a	chr12:40707752-40707761 chr12:40707963-40707974
12	BATF	chr12:40707731-40708124	GM12878	blood:	n/a	chr12:40707752-40707761 chr12:40707963-40707974
13	BATF	chr12:40655828-40656026	GM12878	blood:	n/a	chr12:40655963-40655974
14	BATF	chr12:40655840-40656023	GM12878	blood:	n/a	chr12:40655963-40655974
15	BATF	chr12:40656440-40656787	GM12878	blood:	n/a	n/a
16	BCL11A	chr12:40707747-40708026	GM12878	blood:	n/a	n/a
17	BCL11A	chr12:40707762-40708143	GM12878	blood:	n/a	n/a
18	BCL11A	chr12:40656391-40656827	GM12878	blood:	n/a	n/a
19	BCL11A	chr12:40656497-40656736	GM12878	blood:	n/a	n/a
20	BCL3	chr12:40680909-40681796	A549	lung:	n/a	n/a
21	BCL3	chr12:40680963-40681733	A549	lung:	n/a	n/a
22	BCLAF1	chr12:40656342-40656718	GM12878	blood:	n/a	n/a
23	BHLHE40	chr12:40655843-40656217	GM12878	blood:	n/a	n/a
24	BHLHE40	chr12:40656510-40656885	GM12878	blood:	n/a	n/a
25	BHLHE40	chr12:40707654-40708101	GM12878	blood:	n/a	n/a
26	BHLHE40	chr12:40706940-40707092	GM12878	blood:	n/a	n/a
27	CBX3	chr12:40642410-40642763	HCT-116	colon:	n/a	n/a
28	CEBPB	chr12:40630141-40630428	K562	blood:	n/a	chr12:40630267-40630278
29	CEBPB	chr12:40657459-40657766	IMR90	lung:	n/a	n/a
30	CEBPB	chr12:40632127-40632489	A549	lung:	n/a	chr12:40632271-40632284
31	CEBPB	chr12:40658977-40659258	IMR90	lung:	n/a	n/a
32	CEBPB	chr12:40631962-40632642	Hela-S3	cervix:	n/a	chr12:40632271-40632284
33	CEBPB	chr12:40681486-40681766	A549	lung:	n/a	n/a
34	CEBPB	chr12:40681020-40681637	A549	lung:	n/a	chr12:40681102-40681115
35	CEBPB	chr12:40637428-40637679	HepG2	liver:	n/a	chr12:40637648-40637660 chr12:40637549-40637562 chr12:40637549-40637560 chr12:40637549-40637562
36	CEBPB	chr12:40700006-40700007	A549	lung:	n/a	n/a
37	CEBPB	chr12:40682034-40682312	HepG2	liver:	n/a	chr12:40682155-40682166
38	CEBPB	chr12:40687418-40687571	HepG2	liver:	n/a	chr12:40687473-40687484 chr12:40687474-40687485 chr12:40687473-40687484 chr12:40687475-40687484 chr12:40687475-40687484 chr12:40687475-40687484 chr12:40687473-40687486 chr12:40687475-40687484
39	CEBPB	chr12:40649106-40649333	HepG2	liver:	n/a	n/a
40	CEBPB	chr12:40680384-40680794	A549	lung:	n/a	n/a
41	CEBPB	chr12:40667713-40667780	HepG2	liver:	n/a	n/a
42	CEBPB	chr12:40682182-40682204	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr12:40681011-40681898	A549	lung:	n/a	chr12:40681102-40681115 chr12:40681841-40681854
44	CEBPB	chr12:40630137-40630417	HepG2	liver:	n/a	chr12:40630267-40630278
45	CEBPB	chr12:40687337-40687550	A549	lung:	n/a	chr12:40687473-40687484 chr12:40687474-40687485 chr12:40687473-40687484 chr12:40687475-40687484 chr12:40687475-40687484 chr12:40687475-40687484 chr12:40687473-40687486 chr12:40687475-40687484
46	CEBPB	chr12:40633038-40633067	A549	lung:	n/a	n/a
47	CEBPB	chr12:40680382-40680776	A549	lung:	n/a	n/a
48	CEBPB	chr12:40682075-40682334	A549	lung:	n/a	chr12:40682155-40682166
49	CEBPB	chr12:40680473-40680753	IMR90	lung:	n/a	n/a
50	CEBPB	chr12:40630189-40630363	H1-hESC	embryonic stem cell:	n/a	chr12:40630267-40630278

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:40645170-40645220	MCF-7	breast:	n/a
2	chr12:40645170-40645220	GM06990	blood:	n/a
3	chr12:40645170-40645220	ovcar-3	ovarian:	n/a
4	chr12:40645170-40645220	HCF	heart:	n/a
5	chr12:40645170-40645220	CMK	blood:	n/a
6	chr12:40645170-40645220	ProgFib	skin:	n/a
7	chr12:40645170-40645220	H1-hESC	embryonic stem cell:	embryo
8	chr12:40645170-40645220	HepG2	liver:	n/a
9	chr12:40645170-40645220	NH-A	brain:	n/a
10	chr12:40645170-40645220	NT2-D1	testis:	n/a
11	chr12:40645170-40645220	HRPEpiC	eye:	n/a
12	chr12:40645170-40645220	K562	blood:	n/a
13	chr12:40645170-40645220	HCPEpiC	choroid plexus:	n/a
14	chr12:40645170-40645220	IMR90	lung:	fetal
15	chr12:40645170-40645220	AG04449	skin:	fetal
16	chr12:40645170-40645220	HCM	heart:	n/a
17	chr12:40645170-40645220	HRE	kidney:	n/a
18	chr12:40645170-40645220	SAEC	small airway:	n/a
19	chr12:40645170-40645220	AG10803	skin:	n/a
20	chr12:40645170-40645220	HMEC	breast:	n/a
21	chr12:40645170-40645220	BJ	skin:	n/a
22	chr12:40645170-40645220	RPTEC	kidney:	n/a
23	chr12:40645170-40645220	SKMC	muscle:	n/a
24	chr12:40645170-40645220	GM19239	blood:	n/a
25	chr12:40645170-40645220	AG09319	gingival:	n/a
26	chr12:40645170-40645220	AG09309	skin:	n/a
27	chr12:40645170-40645220	PrEC	prostate:	n/a
28	chr12:40645170-40645220	HL-60	blood:	n/a
29	chr12:40645170-40645220	T-47D	breast:	n/a
30	chr12:40645170-40645220	HCT-116	colon:	n/a
31	chr12:40645170-40645220	HEK293	kidney:	embryo
32	chr12:40645170-40645220	HUVEC	blood vessel:	n/a
33	chr12:40645170-40645220	NHDF-neo	bronchial:	n/a
34	chr12:40645170-40645220	A549	lung:	n/a
35	chr12:40645170-40645220	LNCaP	prostate:	n/a
36	chr12:40645170-40645220	PANC-1	pancreas:	n/a
37	chr12:40645170-40645220	ECC-1	luminal epithelium:	n/a
38	chr12:40645170-40645220	Hela-S3	cervix:	n/a
39	chr12:40645170-40645220	HIPEpiC	eye:	n/a
40	chr12:40645170-40645220	HAEpiC	amniotic membrane:	n/a
41	chr12:40645170-40645220	NB4	blood:	n/a
42	chr12:40645170-40645220	SK-N-SH_RA	brain:	n/a
43	chr12:40645170-40645220	HRCEpiC	kidney:	n/a
44	chr12:40645170-40645220	MCF10A-Er-Src	breast:	n/a
45	chr12:40645170-40645220	PFSK-1	brain:	n/a
46	chr12:40645170-40645220	U87	brain:	n/a
47	chr12:40645170-40645220	AoSMC	blood vessel:	n/a
48	chr12:40645170-40645220	Caco-2	colon:	n/a
49	chr12:40645170-40645220	Hepatocyte	liver:	n/a
50	chr12:40645170-40645220	HPAEpiC	pulmonary alveolar:	n/a

No.	Distal block	Cell Line	Cell type
1	12:40642938-40650987..12:40793507-40812339	K562	blood:
2	chr12:40658480..40661049-chr12:40663809..40666158,2	MCF-7	breast:
3	chr12:40616874..40619503-chr12:40632557..40634590,2	MCF-7	breast:
4	chr12:40546325..40546967-chr12:40662693..40663558,3	MCF-7	breast:
5	chr12:40658480..40661049-chr12:40663809..40666158,2	MCF-7	breast:
6	chr1:153939261..153941119-chr12:40643887..40646371,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000229899	TF binding region
LRRK2	TF binding region
ENSG00000229899	CpG island
LRRK2	CpG island
ENSG00000188906	chromatin interactions
ENSG00000143578	chromatin interactions
ENSG00000205592	chromatin interactions
ENSG00000143570	chromatin interactions
ENSG00000225342	chromatin interactions

Extended variants
information (count: 3346 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:3346 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11564154	chr12:40629636-40629637	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs556307450	chr12:40629639-40629640	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs541732919	chr12:40629687-40629688	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs566312280	chr12:40629723-40629724	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs374837297	chr12:40629728-40629729	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs575045385	chr12:40629738-40629739	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs117297508	chr12:40629747-40629748	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs554495013	chr12:40629749-40629750	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs572665461	chr12:40629768-40629769	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs2723269	chr12:40629787-40629788	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs377641919	chr12:40629848-40629849	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs577034496	chr12:40629849-40629850	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs537070941	chr12:40629887-40629888	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs558489463	chr12:40629897-40629898	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs28365212	chr12:40629915-40629916	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs562328191	chr12:40629917-40629918	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs192190564	chr12:40629939-40629940	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs142565063	chr12:40629994-40629995	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs560058349	chr12:40630006-40630007	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs113752248	chr12:40630007-40630008	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs149349059	chr12:40630189-40630190	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs527443423	chr12:40630209-40630210	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs572713468	chr12:40630226-40630227	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs551957469	chr12:40630233-40630234	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs570586537	chr12:40630273-40630274	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs146013907	chr12:40630325-40630326	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs550286059	chr12:40630335-40630336	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs568344167	chr12:40630337-40630338	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs184748981	chr12:40630338-40630339	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs189610775	chr12:40630366-40630367	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs554463183	chr12:40630385-40630386	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs148688135	chr12:40630388-40630389	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs540007967	chr12:40630396-40630397	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs558398823	chr12:40630404-40630405	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs193005154	chr12:40630459-40630460	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs553779167	chr12:40630584-40630585	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs74700091	chr12:40630597-40630598	Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs556272005	chr12:40630607-40630608	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs11564115	chr12:40630639-40630640	Weak transcription Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs373622326	chr12:40630657-40630658	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs184310879	chr12:40630658-40630659	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs542439627	chr12:40630665-40630666	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs554675076	chr12:40630716-40630717	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs559824243	chr12:40630725-40630726	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs144652202	chr12:40630757-40630758	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs576175153	chr12:40630814-40630815	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs563926119	chr12:40630857-40630858	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs531563331	chr12:40630904-40630905	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs142238241	chr12:40630905-40630906	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs555244787	chr12:40630916-40630917	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

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
Cancer	20164919	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
Autism	20858243	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Cancer	20164920	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:526 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:40619400-40634600	Weak transcription	Spleen	Spleen
2	chr12:40619400-40644400	Weak transcription	Gastric	stomach
3	chr12:40619600-40636400	Weak transcription	Fetal Muscle Leg	muscle
4	chr12:40619600-40661000	Weak transcription	Sigmoid Colon	Sigmoid Colon
5	chr12:40619600-40678400	Weak transcription	Right Ventricle	heart
6	chr12:40619800-40658800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr12:40620400-40630000	Weak transcription	Ovary	ovary
8	chr12:40620400-40644200	Weak transcription	Brain Angular Gyrus	brain
9	chr12:40620800-40634800	Weak transcription	Lung	lung
10	chr12:40620800-40634800	Weak transcription	Pancreas	Pancrea
11	chr12:40620800-40644200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
12	chr12:40620800-40648000	Weak transcription	Skeletal Muscle Male	skeletal muscle
13	chr12:40620800-40659200	Weak transcription	Brain Anterior Caudate	brain
14	chr12:40620800-40704200	Weak transcription	Esophagus	oesophagus
15	chr12:40621000-40630200	Weak transcription	Duodenum Smooth Muscle	Duodenum
16	chr12:40621000-40632000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr12:40621000-40643800	Weak transcription	Stomach Smooth Muscle	stomach
18	chr12:40621000-40659800	Weak transcription	Rectal Mucosa Donor 29	rectum
19	chr12:40621000-40661200	Weak transcription	Rectal Smooth Muscle	rectum
20	chr12:40621200-40631800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr12:40621200-40632000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr12:40621400-40632400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr12:40622800-40661000	Weak transcription	Colon Smooth Muscle	Colon
24	chr12:40622800-40708800	Weak transcription	Left Ventricle	heart
25	chr12:40624600-40631200	Weak transcription	A549	lung
26	chr12:40626400-40630000	Strong transcription	Primary monocytes fromperipheralblood	blood
27	chr12:40626600-40630600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
28	chr12:40628000-40631400	Strong transcription	Monocytes-CD14+_RO01746	blood
29	chr12:40628200-40629800	Weak transcription	Liver	Liver
30	chr12:40628200-40631400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
31	chr12:40628400-40632000	Strong transcription	Primary B cells from cord blood	blood
32	chr12:40628800-40631200	Strong transcription	Skeletal Muscle Female	skeletal muscle
33	chr12:40629000-40630600	Genic enhancers	Primary neutrophils fromperipheralblood	blood
34	chr12:40629200-40633400	Strong transcription	Adipose Nuclei	Adipose
35	chr12:40629200-40635600	Weak transcription	Rectal Mucosa Donor 31	rectum
36	chr12:40629400-40632200	Strong transcription	Primary B cells from peripheral blood	blood
37	chr12:40629600-40630000	Weak transcription	Aorta	Aorta
38	chr12:40629800-40631200	Strong transcription	Liver	Liver
39	chr12:40630000-40630600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr12:40630000-40630600	Strong transcription	Aorta	Aorta
41	chr12:40630000-40630600	Strong transcription	Ovary	ovary
42	chr12:40630000-40632000	Genic enhancers	Primary monocytes fromperipheralblood	blood
43	chr12:40630200-40630600	Strong transcription	Duodenum Smooth Muscle	Duodenum
44	chr12:40630600-40631400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr12:40630600-40633000	Weak transcription	Aorta	Aorta
46	chr12:40630600-40633000	Weak transcription	Ovary	ovary
47	chr12:40630600-40643600	Weak transcription	Duodenum Smooth Muscle	Duodenum
48	chr12:40630600-40669400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
49	chr12:40630600-40686400	Strong transcription	Primary neutrophils fromperipheralblood	blood
50	chr12:40631000-40633200	Enhancers	Hela-S3	cervix

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