Variant report

Variant	nsv976602
Chromosome Location	chr12:38676673-38718735
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:833)
CpG islands
(count:733)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:38710301-38710555	K562	blood:	n/a	n/a
2	ARID3A	chr12:38710113-38710696	HepG2	liver:	n/a	chr12:38710204-38710220 chr12:38710205-38710221
3	ATF1	chr12:38710296-38710661	K562	blood:	n/a	n/a
4	ATF2	chr12:38710159-38710775	GM12878	blood:	n/a	n/a
5	ATF2	chr12:38710293-38710713	GM12878	blood:	n/a	n/a
6	ATF3	chr12:38710219-38710780	A549	lung:	n/a	n/a
7	ATF3	chr12:38710223-38710780	A549	lung:	n/a	n/a
8	BATF	chr12:38710371-38710641	GM12878	blood:	n/a	n/a
9	BATF	chr12:38710378-38710679	GM12878	blood:	n/a	n/a
10	BCL11A	chr12:38710258-38710721	GM12878	blood:	n/a	n/a
11	BCL3	chr12:38710209-38710812	A549	lung:	n/a	n/a
12	BCL3	chr12:38710141-38710775	A549	lung:	n/a	n/a
13	BCLAF1	chr12:38710352-38710785	K562	blood:	n/a	n/a
14	BCLAF1	chr12:38710117-38710847	GM12878	blood:	n/a	n/a
15	BCLAF1	chr12:38710098-38710795	GM12878	blood:	n/a	n/a
16	BHLHE40	chr12:38710409-38710609	K562	blood:	n/a	n/a
17	BHLHE40	chr12:38710156-38710702	GM12878	blood:	n/a	n/a
18	BHLHE40	chr12:38710353-38710663	HepG2	liver:	n/a	n/a
19	BRCA1	chr12:38710358-38710669	GM12878	blood:	n/a	n/a
20	BRCA1	chr12:38718322-38719076	Hela-S3	cervix:	n/a	n/a
21	BRCA1	chr12:38710387-38710653	HepG2	liver:	n/a	n/a
22	BRCA1	chr12:38710312-38710651	H1-hESC	embryonic stem cell:	n/a	n/a
23	BRCA1	chr12:38709964-38710766	Hela-S3	cervix:	n/a	n/a
24	CBX3	chr12:38710156-38710688	K562	blood:	n/a	n/a
25	CBX3	chr12:38710216-38710780	HCT-116	colon:	n/a	n/a
26	CBX3	chr12:38710362-38710671	K562	blood:	n/a	n/a
27	CBX3	chr12:38710189-38710797	HCT-116	colon:	n/a	n/a
28	CBX3	chr12:38676620-38677125	HCT-116	colon:	n/a	n/a
29	CBX3	chr12:38676688-38677104	HCT-116	colon:	n/a	n/a
30	CEBPB	chr12:38710276-38710636	A549	lung:	n/a	n/a
31	CEBPB	chr12:38676649-38676990	HCT-116	colon:	n/a	n/a
32	CEBPB	chr12:38682679-38682858	HepG2	liver:	n/a	chr12:38682790-38682807
33	CEBPB	chr12:38710260-38710638	IMR90	lung:	n/a	n/a
34	CEBPB	chr12:38710380-38710639	ECC-1	luminal epithelium:	n/a	n/a
35	CEBPB	chr12:38710148-38710725	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr12:38710317-38710514	HepG2	liver:	n/a	n/a
37	CEBPB	chr12:38710313-38710628	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr12:38676656-38677027	ECC-1	luminal epithelium:	n/a	n/a
39	CEBPB	chr12:38710243-38710659	MCF-7	breast:	n/a	n/a
40	CEBPB	chr12:38710226-38710745	ECC-1	luminal epithelium:	n/a	n/a
41	CEBPB	chr12:38710252-38710620	HepG2	liver:	n/a	n/a
42	CEBPB	chr12:38710325-38710629	A549	lung:	n/a	n/a
43	CEBPB	chr12:38676597-38677149	HCT-116	colon:	n/a	n/a
44	CEBPB	chr12:38710448-38710664	GM12878	blood:	n/a	n/a
45	CEBPB	chr12:38710170-38710764	GM12878	blood:	n/a	n/a
46	CEBPB	chr12:38710382-38710584	K562	blood:	n/a	n/a
47	CEBPB	chr12:38710315-38710609	K562	blood:	n/a	n/a
48	CEBPB	chr12:38684781-38684902	HepG2	liver:	n/a	chr12:38684791-38684802
49	CEBPB	chr12:38710176-38710750	A549	lung:	n/a	n/a
50	CEBPB	chr12:38718296-38719186	Hela-S3	cervix:	n/a	n/a

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:38710700-38710750	HPAEpiC	pulmonary alveolar:	n/a
2	chr12:38710700-38710750	HPAEpiC	pulmonary alveolar:	n/a
3	chr12:38710604-38710654	HL-60	blood:	n/a
4	chr12:38710491-38710541	AG09309	skin:	n/a
5	chr12:38714149-38714199	AG10803	skin:	n/a
6	chr12:38710408-38710458	HepG2	liver:	n/a
7	chr12:38710953-38711003	Hepatocyte	liver:	n/a
8	chr12:38714149-38714199	SK-N-MC	brain:	n/a
9	chr12:38710504-38710554	HMEC	breast:	n/a
10	chr12:38710504-38710554	SK-N-SH_RA	brain:	n/a
11	chr12:38710700-38710750	H1-hESC	embryonic stem cell:	embryo
12	chr12:38710408-38710458	ovcar-3	ovarian:	n/a
13	chr12:38714149-38714199	H1-hESC	embryonic stem cell:	embryo
14	chr12:38710408-38710458	HUVEC	blood vessel:	n/a
15	chr12:38714149-38714199	Caco-2	colon:	n/a
16	chr12:38710452-38710502	HepG2	liver:	n/a
17	chr12:38710424-38710474	HCM	heart:	n/a
18	chr12:38710408-38710458	NH-A	brain:	n/a
19	chr12:38710424-38710474	HL-60	blood:	n/a
20	chr12:38710504-38710554	AG09319	gingival:	n/a
21	chr12:38714149-38714199	NHBE	bronchial:	n/a
22	chr12:38714149-38714199	PFSK-1	brain:	n/a
23	chr12:38710504-38710554	HRPEpiC	eye:	n/a
24	chr12:38710408-38710458	NHDF-neo	bronchial:	n/a
25	chr12:38710424-38710474	NHDF-neo	bronchial:	n/a
26	chr12:38710154-38710204	AG10803	skin:	n/a
27	chr12:38710154-38710204	GM06990	blood:	n/a
28	chr12:38710953-38711003	ovcar-3	ovarian:	n/a
29	chr12:38714149-38714199	T-47D	breast:	n/a
30	chr12:38710424-38710474	MCF-7	breast:	n/a
31	chr12:38710604-38710654	NHDF-neo	bronchial:	n/a
32	chr12:38710154-38710204	Caco-2	colon:	n/a
33	chr12:38710491-38710541	HL-60	blood:	n/a
34	chr12:38710433-38710483	NHBE	bronchial:	n/a
35	chr12:38710424-38710474	HepG2	liver:	n/a
36	chr12:38710433-38710483	GM12878	blood:	n/a
37	chr12:38710452-38710502	HCPEpiC	choroid plexus:	n/a
38	chr12:38710953-38711003	PANC-1	pancreas:	n/a
39	chr12:38710606-38710656	HEEpiC	esophagus:	n/a
40	chr12:38710606-38710656	HepG2	liver:	n/a
41	chr12:38710154-38710204	T-47D	breast:	n/a
42	chr12:38710504-38710554	A549	lung:	n/a
43	chr12:38710408-38710458	HL-60	blood:	n/a
44	chr12:38714149-38714199	LNCaP	prostate:	n/a
45	chr12:38710408-38710458	SK-N-MC	brain:	n/a
46	chr12:38710154-38710204	HUVEC	blood vessel:	n/a
47	chr12:38710504-38710554	HCM	heart:	n/a
48	chr12:38710606-38710656	MCF10A-Er-Src	breast:	n/a
49	chr12:38710491-38710541	CMK	blood:	n/a
50	chr12:38710953-38711003	HAEpiC	amniotic membrane:	n/a

(count:2 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:34175001..34175865-chr12:38710413..38711151,3	HCT-116	colon:
2	chr12:38676913..38678502-chr12:38709612..38711993,2	MCF-7	breast:

No data

Variant related genes	Relation type
ALG10B	TF binding region
ENSG00000266333	TF binding region
ALG10B	CpG island
ENSG00000266333	CpG island
ENSG00000175548	chromatin interactions
ENSG00000139133	chromatin interactions

Extended variants
information (count: 1306 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:1306 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11183160	chr12:38676702-38676703	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs12298726	chr12:38676710-38676711	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs571406617	chr12:38676726-38676727	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs533633152	chr12:38676828-38676829	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs546199949	chr12:38676855-38676856	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs557831906	chr12:38676901-38676902	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs114296561	chr12:38676941-38676942	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs181117002	chr12:38676978-38676979	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs555796774	chr12:38676982-38676983	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs575488543	chr12:38677072-38677073	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs138910850	chr12:38677127-38677128	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs186862974	chr12:38677128-38677129	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs564012784	chr12:38677133-38677134	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs577749939	chr12:38677274-38677275	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs188808497	chr12:38677292-38677293	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs181486483	chr12:38677399-38677400	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs1843910	chr12:38677408-38677409	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs375393350	chr12:38677412-38677413	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs117103431	chr12:38677413-38677414	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs562817335	chr12:38677416-38677417	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs531627033	chr12:38677420-38677421	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs142818156	chr12:38677423-38677424	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs112483645	chr12:38677490-38677491	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs146982568	chr12:38677500-38677501	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs527249612	chr12:38677547-38677548	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs547188587	chr12:38677559-38677560	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs528977793	chr12:38677560-38677561	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs567311792	chr12:38677576-38677577	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs141660984	chr12:38677626-38677627	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs77715030	chr12:38677627-38677628	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs569253761	chr12:38677631-38677632	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs538136177	chr12:38677661-38677662	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs557757687	chr12:38677685-38677686	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs111868039	chr12:38677691-38677692	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs370082061	chr12:38677710-38677711	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs534164421	chr12:38677753-38677754	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs576647505	chr12:38677763-38677764	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs574074787	chr12:38677781-38677782	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs542496896	chr12:38677881-38677882	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs550934444	chr12:38677884-38677885	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs61162973	chr12:38677890-38677891	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs576430393	chr12:38677902-38677903	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs545341710	chr12:38677903-38677904	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs565140864	chr12:38677941-38677942	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs563083053	chr12:38677955-38677956	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs527297122	chr12:38677981-38677982	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs547324826	chr12:38677999-38678000	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs560868458	chr12:38678006-38678007	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs529790234	chr12:38678035-38678036	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs549203597	chr12:38678056-38678057	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:57)

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
Breast cancer	21509527	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
Breast cancer	21364760	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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:401 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:38675200-38676800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr12:38675200-38677400	Enhancers	HMEC	breast
3	chr12:38675800-38677000	Enhancers	NHEK	skin
4	chr12:38675800-38677800	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr12:38676800-38677200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr12:38677200-38678000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr12:38677400-38677600	Weak transcription	HMEC	breast
8	chr12:38677600-38678000	Enhancers	HMEC	breast
9	chr12:38678000-38682600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr12:38678000-38682600	Weak transcription	HMEC	breast
11	chr12:38682600-38683600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr12:38682600-38683600	Enhancers	HMEC	breast
13	chr12:38683600-38696200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr12:38688400-38688600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr12:38690000-38690600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr12:38696200-38696600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr12:38701000-38701200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr12:38709400-38709800	Enhancers	HUVEC	blood vessel
19	chr12:38709400-38710000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr12:38709600-38709800	Enhancers	Breast Myoepithelial Primary Cells	Breast
21	chr12:38709600-38709800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
22	chr12:38709600-38709800	Enhancers	Adipose Nuclei	Adipose
23	chr12:38709600-38709800	Enhancers	Brain Anterior Caudate	brain
24	chr12:38709600-38709800	Enhancers	Brain Hippocampus Middle	brain
25	chr12:38709600-38709800	Enhancers	NHDF-Ad	bronchial
26	chr12:38709600-38710000	Enhancers	Primary T helper naive cells from peripheral blood	blood
27	chr12:38709600-38710000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr12:38709600-38710000	Enhancers	Dnd41	blood
29	chr12:38709600-38710000	Enhancers	Hela-S3	cervix
30	chr12:38709600-38710800	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr12:38709800-38710000	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
32	chr12:38709800-38710000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
33	chr12:38709800-38710000	Enhancers	Primary T helper cells PMA-I stimulated	--
34	chr12:38709800-38710000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
35	chr12:38709800-38710000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
36	chr12:38709800-38710000	Enhancers	Muscle Satellite Cultured Cells	--
37	chr12:38709800-38710000	Enhancers	Liver	Liver
38	chr12:38709800-38710000	Enhancers	Brain Cingulate Gyrus	brain
39	chr12:38709800-38710000	Flanking Active TSS	Brain Hippocampus Middle	brain
40	chr12:38709800-38710000	Enhancers	Fetal Lung	lung
41	chr12:38709800-38710000	Enhancers	HMEC	breast
42	chr12:38709800-38710000	Active TSS	HUVEC	blood vessel
43	chr12:38709800-38710200	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
44	chr12:38709800-38710200	Flanking Active TSS	Adipose Nuclei	Adipose
45	chr12:38709800-38710200	Flanking Active TSS	Brain Anterior Caudate	brain
46	chr12:38709800-38710400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
47	chr12:38709800-38710600	Active TSS	Primary hematopoietic stem cells	blood
48	chr12:38709800-38711000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr12:38709800-38711000	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr12:38709800-38711000	Active TSS	Brain Inferior Temporal Lobe	brain

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