Variant report

Variant	nsv557755
Chromosome Location	chr12:22059617-22072257
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	chr12:22064893-22065547	IMR90	lung:	n/a	chr12:22065069-22065080
2	CEBPB	chr12:22064939-22065123	H1-hESC	embryonic stem cell:	n/a	chr12:22065069-22065080
3	CEBPB	chr12:22064894-22065168	K562	blood:	n/a	chr12:22065069-22065080
4	CEBPB	chr12:22064922-22065195	HepG2	liver:	n/a	chr12:22065069-22065080
5	CEBPB	chr12:22064865-22065268	K562	blood:	n/a	chr12:22065069-22065080
6	CTCF	chr12:22060163-22060363	GM12878	blood:	n/a	n/a
7	E2F4	chr12:22065284-22065500	MCF10A-Er-Src	breast:	n/a	n/a
8	EP300	chr12:22059811-22059995	GM12878	blood:	n/a	n/a
9	FOS	chr12:22064849-22065717	MCF10A-Er-Src	breast:	n/a	chr12:22065448-22065456 chr12:22065447-22065457 chr12:22065447-22065457 chr12:22065447-22065457
10	FOS	chr12:22065023-22065708	MCF10A-Er-Src	breast:	n/a	chr12:22065448-22065456 chr12:22065447-22065457 chr12:22065447-22065457 chr12:22065447-22065457
11	FOS	chr12:22066813-22067168	MCF10A-Er-Src	breast:	n/a	chr12:22066991-22067001 chr12:22066992-22067000 chr12:22066992-22066999 chr12:22066991-22067001 chr12:22066992-22067000
12	FOS	chr12:22066188-22067356	MCF10A-Er-Src	breast:	n/a	chr12:22066991-22067001 chr12:22066992-22067000 chr12:22066992-22066999 chr12:22066991-22067001 chr12:22066992-22067000
13	FOS	chr12:22066801-22067309	MCF10A-Er-Src	breast:	n/a	chr12:22066991-22067001 chr12:22066992-22067000 chr12:22066992-22066999 chr12:22066991-22067001 chr12:22066992-22067000
14	FOS	chr12:22066134-22066537	MCF10A-Er-Src	breast:	n/a	n/a
15	FOS	chr12:22065211-22065643	MCF10A-Er-Src	breast:	n/a	chr12:22065448-22065456 chr12:22065447-22065457 chr12:22065447-22065457 chr12:22065447-22065457
16	FOS	chr12:22066810-22067211	MCF10A-Er-Src	breast:	n/a	chr12:22066991-22067001 chr12:22066992-22067000 chr12:22066992-22066999 chr12:22066991-22067001 chr12:22066992-22067000
17	FOS	chr12:22065198-22065626	MCF10A-Er-Src	breast:	n/a	chr12:22065448-22065456 chr12:22065447-22065457 chr12:22065447-22065457 chr12:22065447-22065457
18	FOS	chr12:22066180-22066590	MCF10A-Er-Src	breast:	n/a	n/a
19	MYC	chr12:22066818-22067207	MCF10A-Er-Src	breast:	n/a	n/a
20	MYC	chr12:22064978-22065608	MCF10A-Er-Src	breast:	n/a	n/a
21	POLR2A	chr12:22070329-22070385	MCF10A-Er-Src	breast:	n/a	n/a
22	POLR2A	chr12:22069583-22069740	MCF10A-Er-Src	breast:	n/a	n/a
23	POLR2A	chr12:22066236-22066569	MCF10A-Er-Src	breast:	n/a	n/a
24	POLR2A	chr12:22065371-22065433	MCF10A-Er-Src	breast:	n/a	n/a
25	POLR2A	chr12:22067312-22067410	MCF10A-Er-Src	breast:	n/a	n/a
26	POLR2A	chr12:22064940-22065079	MCF10A-Er-Src	breast:	n/a	n/a
27	POLR2A	chr12:22067613-22067793	MCF10A-Er-Src	breast:	n/a	n/a
28	STAT3	chr12:22064980-22067736	MCF10A-Er-Src	breast:	n/a	chr12:22066079-22066087 chr12:22066752-22066759
29	STAT3	chr12:22064496-22064577	MCF10A-Er-Src	breast:	n/a	n/a
30	STAT3	chr12:22064850-22065765	MCF10A-Er-Src	breast:	n/a	n/a
31	STAT3	chr12:22065839-22065859	MCF10A-Er-Src	breast:	n/a	n/a
32	STAT3	chr12:22066814-22067263	MCF10A-Er-Src	breast:	n/a	n/a
33	STAT3	chr12:22069882-22070008	MCF10A-Er-Src	breast:	n/a	n/a
34	STAT3	chr12:22061931-22062122	MCF10A-Er-Src	breast:	n/a	chr12:22062036-22062044
35	STAT3	chr12:22064879-22065764	MCF10A-Er-Src	breast:	n/a	n/a
36	STAT3	chr12:22064879-22065716	MCF10A-Er-Src	breast:	n/a	n/a
37	STAT3	chr12:22060774-22060864	MCF10A-Er-Src	breast:	n/a	n/a
38	STAT3	chr12:22066135-22067406	MCF10A-Er-Src	breast:	n/a	chr12:22066752-22066759
39	STAT3	chr12:22066016-22067689	MCF10A-Er-Src	breast:	n/a	chr12:22066079-22066087 chr12:22066752-22066759
40	STAT3	chr12:22066015-22067703	MCF10A-Er-Src	breast:	n/a	chr12:22066079-22066087 chr12:22066752-22066759
41	STAT3	chr12:22065383-22065611	MCF10A-Er-Src	breast:	n/a	n/a
42	STAT3	chr12:22068739-22068773	MCF10A-Er-Src	breast:	n/a	n/a
43	STAT3	chr12:22062383-22062588	MCF10A-Er-Src	breast:	n/a	n/a
44	TAL1	chr12:22064785-22065131	K562	blood:	n/a	n/a
45	TCF12	chr12:22059933-22060364	SK-N-SH	brain:	n/a	n/a
46	TCF12	chr12:22059830-22060399	SK-N-SH	brain:	n/a	chr12:22060384-22060393 chr12:22059872-22059879
47	TEAD4	chr12:22063581-22063953	H1-hESC	embryonic stem cell:	n/a	n/a
48	TEAD4	chr12:22063611-22063971	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:22061241..22063260-chr12:22065386..22067190,2	K562	blood:
2	chr12:22061241..22063351-chr12:22065690..22068312,2	K562	blood:
3	chr12:22061241..22063260-chr12:22065386..22067190,2	K562	blood:
4	chr12:22061241..22063351-chr12:22065690..22068312,2	K562	blood:

Variant related genes	Relation type
ABCC9	TF binding region

Extended variants
information (count: 502 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:502 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4148660	chr12:22059617-22059618	Strong transcription Flanking Active TSS Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs377310737	chr12:22059629-22059630	Strong transcription Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs548392757	chr12:22059732-22059733	Strong transcription Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs561921910	chr12:22059804-22059805	Strong transcription Flanking Active TSS Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs528010019	chr12:22059857-22059858	Strong transcription Flanking Active TSS Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs10743427	chr12:22059861-22059862	Strong transcription Flanking Active TSS Active TSS Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs373721415	chr12:22059870-22059871	Strong transcription Flanking Active TSS Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs191293025	chr12:22059980-22059981	Strong transcription Flanking Active TSS Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs549469638	chr12:22060001-22060002	Strong transcription Flanking Active TSS Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs11046230	chr12:22060023-22060024	Strong transcription Flanking Active TSS Active TSS Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs185056165	chr12:22060182-22060183	Strong transcription Flanking Active TSS Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs113368719	chr12:22060185-22060186	Strong transcription Flanking Active TSS Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs190557493	chr12:22060219-22060220	Strong transcription Genic enhancers Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs565864735	chr12:22060240-22060241	Strong transcription Genic enhancers Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs1826365	chr12:22060248-22060249	Strong transcription Genic enhancers Flanking Active TSS Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs141591940	chr12:22060260-22060261	Strong transcription Genic enhancers Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs535652816	chr12:22060280-22060281	Strong transcription Genic enhancers Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs577806861	chr12:22060287-22060288	Strong transcription Genic enhancers Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs546267227	chr12:22060346-22060347	Strong transcription Genic enhancers Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs150714831	chr12:22060381-22060382	Strong transcription Genic enhancers Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs576361252	chr12:22060388-22060389	Strong transcription Genic enhancers Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs541840690	chr12:22060400-22060401	Strong transcription Genic enhancers Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs4148659	chr12:22060426-22060427	Strong transcription Genic enhancers Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs527983959	chr12:22060490-22060491	Strong transcription Genic enhancers Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs372872923	chr12:22060510-22060511	Strong transcription Genic enhancers Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs541373872	chr12:22060547-22060548	Strong transcription Genic enhancers Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs564694444	chr12:22060572-22060573	Strong transcription Genic enhancers Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs533396610	chr12:22060577-22060578	Strong transcription Genic enhancers Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs549826409	chr12:22060613-22060614	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs76246098	chr12:22060615-22060616	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs79632053	chr12:22060668-22060669	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs549008955	chr12:22060693-22060694	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs541511965	chr12:22060709-22060710	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs112243367	chr12:22060714-22060715	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs534911305	chr12:22060731-22060732	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs370274674	chr12:22060769-22060770	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs115606421	chr12:22060786-22060787	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs34193205	chr12:22060798-22060799	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs536875288	chr12:22060827-22060828	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs556590625	chr12:22060838-22060839	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs1492135	chr12:22060856-22060857	Strong transcription Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs541777461	chr12:22060857-22060858	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs375478426	chr12:22060986-22060987	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs369553899	chr12:22060996-22060997	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs376587222	chr12:22061007-22061008	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs387907211	chr12:22061033-22061034	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs142219855	chr12:22061065-22061066	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs368698007	chr12:22061068-22061069	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs555340137	chr12:22061070-22061071	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs374535641	chr12:22061085-22061086	Strong transcription Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Malignant germ cell tumour	17285132	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Myxofibrosarcoma	16751306	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Acute myeloid leukemia	16864856	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Testicular cancer	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Seminomas	18059402	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
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
Acute lymphoblastic leukemia	21248843	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	16397240	CNVD
Neurodevelopmental disorder	22521361	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	21509527	CNVD
Autism	22102821	CNVD
Follicular lymphoma	18703704	CNVD
Lung cancer	18438408	CNVD
Lung cancer	21911935	CNVD
Breast cancer	22048815	CNVD
Malignant peripheral nerve sheath tumor	19844265	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Heart disease	21282601	CNVD
Ovarian cancer	20844748	CNVD
Lung cancer	17925434	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Gastric cancer	24379144	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Gastric cancer	19545448	CNVD
Lung cancer	20031968	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung adenocarcinoma	19826477	CNVD
Lung cancer	19525976	CNVD
Lung cancer	19826477	CNVD
Non-small cell lung cancer	19451690	CNVD
Non-small cell lung cancer	17504988	CNVD
Bipolar disorder	19114987	CNVD
Lung cancer	19671679	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	21364760	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:22035200-22092200	Weak transcription	Fetal Muscle Leg	muscle
2	chr12:22045400-22064800	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr12:22045600-22064800	Weak transcription	Fetal Heart	heart
4	chr12:22048000-22092000	Weak transcription	Psoas Muscle	Psoas
5	chr12:22048400-22060000	Weak transcription	Adipose Nuclei	Adipose
6	chr12:22048400-22091600	Weak transcription	Skeletal Muscle Male	skeletal muscle
7	chr12:22049400-22061600	Weak transcription	Fetal Kidney	kidney
8	chr12:22049400-22088600	Weak transcription	Colon Smooth Muscle	Colon
9	chr12:22052600-22060000	Weak transcription	Fetal Lung	lung
10	chr12:22058000-22061200	Weak transcription	Ovary	ovary
11	chr12:22058000-22065200	Strong transcription	Skeletal Muscle Female	skeletal muscle
12	chr12:22058400-22061200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr12:22058400-22062000	Strong transcription	Stomach Smooth Muscle	stomach
14	chr12:22058600-22060200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr12:22058800-22060800	Strong transcription	Fetal Muscle Trunk	muscle
16	chr12:22059000-22061200	Strong transcription	Duodenum Smooth Muscle	Duodenum
17	chr12:22059200-22060000	Enhancers	Muscle Satellite Cultured Cells	--
18	chr12:22059200-22060200	Enhancers	Osteobl	bone
19	chr12:22059200-22060600	Enhancers	NHLF	lung
20	chr12:22059200-22061800	Strong transcription	Left Ventricle	heart
21	chr12:22059200-22062600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr12:22059400-22059800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr12:22059400-22091800	Weak transcription	Liver	Liver
24	chr12:22059600-22060400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr12:22059600-22060400	Flanking Active TSS	NHDF-Ad	bronchial
26	chr12:22059800-22060200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr12:22059800-22060400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr12:22059800-22060600	Enhancers	NH-A	brain
29	chr12:22060000-22060400	Flanking Active TSS	Muscle Satellite Cultured Cells	--
30	chr12:22060000-22060400	Enhancers	Adipose Nuclei	Adipose
31	chr12:22060000-22060600	Enhancers	Fetal Lung	lung
32	chr12:22060200-22060400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr12:22060200-22060600	Genic enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr12:22060200-22064600	Weak transcription	Osteobl	bone
35	chr12:22060400-22060600	Flanking Active TSS	Adipose Nuclei	Adipose
36	chr12:22060400-22060800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr12:22060400-22060800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr12:22060400-22061200	Enhancers	Muscle Satellite Cultured Cells	--
39	chr12:22060400-22061200	Enhancers	NHDF-Ad	bronchial
40	chr12:22060400-22064600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr12:22060600-22061600	Enhancers	Adipose Nuclei	Adipose
42	chr12:22060600-22063600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr12:22060600-22064800	Weak transcription	NH-A	brain
44	chr12:22060600-22065800	Weak transcription	NHLF	lung
45	chr12:22060800-22065000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr12:22060800-22065000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr12:22060800-22092200	Weak transcription	Fetal Muscle Trunk	muscle
48	chr12:22061200-22062400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr12:22061200-22062600	Weak transcription	NHDF-Ad	bronchial
50	chr12:22061200-22063000	Enhancers	Brain Germinal Matrix	brain

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