Variant report

Variant	nsv894712
Chromosome Location	chr10:595504-631041
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:147)
CpG islands
(count:1345)
Chromatin interactive
region (count:24)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:147 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr10:603849-604150	H1-hESC	embryonic stem cell:	n/a	chr10:603936-603945
2	ATF3	chr10:603843-604054	K562	blood:	n/a	chr10:603936-603945
3	BHLHE40	chr10:629787-629980	K562	blood:	n/a	chr10:629835-629844 chr10:629836-629845 chr10:629835-629844
4	CEBPB	chr10:626623-627083	IMR90	lung:	n/a	n/a
5	CEBPB	chr10:617766-618133	IMR90	lung:	n/a	n/a
6	CHD2	chr10:601726-601734	H1-hESC	embryonic stem cell:	n/a	n/a
7	CTCF	chr10:619380-619530	HepG2	liver:	n/a	n/a
8	CTCF	chr10:619380-619530	HAc	cerebellar:	n/a	n/a
9	CTCF	chr10:619261-619474	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTCF	chr10:619304-619505	MCF-7	breast:	n/a	n/a
11	CTCF	chr10:619287-619529	K562	blood:	n/a	n/a
12	CTCF	chr10:603380-603530	SK-N-SH_RA	brain:	n/a	n/a
13	CTCF	chr10:619322-619487	MCF-7	breast:	n/a	n/a
14	CTCF	chr10:619320-619470	Caco-2	colon:	n/a	n/a
15	CTCF	chr10:619310-619492	MCF-7	breast:	n/a	n/a
16	CTCF	chr10:615814-615836	GM13976	blood:	n/a	n/a
17	CTCF	chr10:619302-619504	MCF-7	breast:	n/a	n/a
18	CTCF	chr10:619316-619506	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr10:619320-619470	HEK293	kidney:	n/a	n/a
20	CTCF	chr10:619320-619470	K562	blood:	n/a	n/a
21	CTCF	chr10:619305-619505	MCF-7	breast:	n/a	n/a
22	CTCF	chr10:625440-625590	Caco-2	colon:	n/a	n/a
23	CTCF	chr10:612312-612381	H1-hESC	embryonic stem cell:	n/a	chr10:612342-612351
24	CTCF	chr10:619340-619490	HEEpiC	esophagus:	n/a	n/a
25	CTCF	chr10:619380-619530	MCF-7	breast:	n/a	n/a
26	CTCF	chr10:617640-617790	GM12871	blood:	n/a	n/a
27	CTCF	chr10:619340-619490	K562	blood:	n/a	n/a
28	CTCF	chr10:619268-619481	K562	blood:	n/a	n/a
29	CTCF	chr10:619240-619390	HRE	kidney:	n/a	n/a
30	CTCF	chr10:619320-619470	HA-sp	spinal cord:	n/a	n/a
31	CTCF	chr10:619320-619494	K562	blood:	n/a	n/a
32	CTCF	chr10:619320-619470	MCF-7	breast:	n/a	n/a
33	CTCF	chr10:619282-619694	K562	blood:	n/a	n/a
34	E2F4	chr10:606351-606617	MCF10A-Er-Src	breast:	n/a	n/a
35	E2F6	chr10:611603-612141	H1-hESC	embryonic stem cell:	n/a	n/a
36	FOS	chr10:626476-627145	MCF10A-Er-Src	breast:	n/a	chr10:626841-626849 chr10:626938-626949 chr10:626716-626725
37	FOS	chr10:626654-627116	MCF10A-Er-Src	breast:	n/a	chr10:626841-626849 chr10:626938-626949 chr10:626716-626725
38	FOS	chr10:622984-623196	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr10:626670-627095	MCF10A-Er-Src	breast:	n/a	chr10:626841-626849 chr10:626938-626949 chr10:626716-626725
40	FOS	chr10:609736-609833	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr10:626663-627026	MCF10A-Er-Src	breast:	n/a	chr10:626841-626849 chr10:626938-626949 chr10:626716-626725
42	FOS	chr10:622163-622384	MCF10A-Er-Src	breast:	n/a	chr10:622320-622331
43	FOS	chr10:600069-600542	HUVEC	blood vessel:	n/a	chr10:600274-600285
44	FOSL2	chr10:626561-627192	SK-N-SH	brain:	n/a	chr10:626841-626849 chr10:626938-626949 chr10:626716-626725
45	FOSL2	chr10:600011-600587	SK-N-SH	brain:	n/a	n/a
46	FOXA1	chr10:619203-619488	HepG2	liver:	n/a	n/a
47	FOXA1	chr10:619259-619488	HepG2	liver:	n/a	n/a
48	FOXA1	chr10:619268-619515	T-47D	breast:	n/a	n/a
49	FOXA1	chr10:618673-618978	T-47D	breast:	n/a	n/a
50	FOXA1	chr10:619237-619503	T-47D	breast:	n/a	n/a

(count:1345 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:616959-617009	GM19239	blood:	n/a
2	chr10:616995-617045	PrEC	prostate:	n/a
3	chr10:617105-617155	HEK293	kidney:	embryo
4	chr10:616959-617009	GM19239	blood:	n/a
5	chr10:616995-617045	PrEC	prostate:	n/a
6	chr10:617105-617155	HEK293	kidney:	embryo
7	chr10:603950-604000	HEK293	kidney:	embryo
8	chr10:601816-601866	HUVEC	blood vessel:	n/a
9	chr10:604032-604082	HNPCEpiC	eye:	n/a
10	chr10:629565-629615	HCT-116	colon:	n/a
11	chr10:630671-630721	PrEC	prostate:	n/a
12	chr10:603950-604000	ProgFib	skin:	n/a
13	chr10:604461-604511	HCPEpiC	choroid plexus:	n/a
14	chr10:604461-604511	PANC-1	pancreas:	n/a
15	chr10:629582-629632	HRPEpiC	eye:	n/a
16	chr10:604461-604511	ECC-1	luminal epithelium:	n/a
17	chr10:630310-630360	NT2-D1	testis:	n/a
18	chr10:616959-617009	HRPEpiC	eye:	n/a
19	chr10:612266-612316	AG04450	lung:	fetal
20	chr10:601783-601833	HRCEpiC	kidney:	n/a
21	chr10:617105-617155	NH-A	brain:	n/a
22	chr10:629582-629632	GM12878	blood:	n/a
23	chr10:630671-630721	MCF-7	breast:	n/a
24	chr10:612314-612364	NH-A	brain:	n/a
25	chr10:603950-604000	AG10803	skin:	n/a
26	chr10:612391-612441	AG09319	gingival:	n/a
27	chr10:616959-617009	SK-N-MC	brain:	n/a
28	chr10:616995-617045	HRCEpiC	kidney:	n/a
29	chr10:630942-630992	GM19239	blood:	n/a
30	chr10:604032-604082	ProgFib	skin:	n/a
31	chr10:623056-623106	HIPEpiC	eye:	n/a
32	chr10:627679-627729	HCM	heart:	n/a
33	chr10:601816-601866	HPAEpiC	pulmonary alveolar:	n/a
34	chr10:630384-630434	K562	blood:	n/a
35	chr10:604523-604573	HMEC	breast:	n/a
36	chr10:612314-612364	AG10803	skin:	n/a
37	chr10:603950-604000	HRCEpiC	kidney:	n/a
38	chr10:630671-630721	Jurkat	blood:	n/a
39	chr10:629582-629632	AoSMC	blood vessel:	n/a
40	chr10:629565-629615	K562	blood:	n/a
41	chr10:623056-623106	AoSMC	blood vessel:	n/a
42	chr10:630310-630360	HAEpiC	amniotic membrane:	n/a
43	chr10:604461-604511	T-47D	breast:	n/a
44	chr10:612266-612316	GM12878	blood:	n/a
45	chr10:617105-617155	AG09319	gingival:	n/a
46	chr10:601759-601809	U87	brain:	n/a
47	chr10:612314-612364	GM12878	blood:	n/a
48	chr10:601783-601833	HCM	heart:	n/a
49	chr10:629625-629675	Hepatocyte	liver:	n/a
50	chr10:601759-601809	Jurkat	blood:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:614375..617220-chr10:617772..620135,2	K562	blood:
2	chr10:612575..614220-chr10:618732..620715,2	K562	blood:
3	chr10:596165..599651-chr10:599666..603906,4	MCF-7	breast:
4	chr10:604798..606576-chr10:618326..620891,2	MCF-7	breast:
5	chr10:596165..599651-chr10:599666..603906,4	MCF-7	breast:
6	chr10:612575..614220-chr10:618732..620715,2	K562	blood:
7	chr10:614375..617220-chr10:617772..620135,2	K562	blood:
8	chr10:627398..629681-chr10:634831..636887,2	MCF-7	breast:
9	chr10:612084..613939-chr10:620156..623111,2	MCF-7	breast:
10	chr10:620907..622764-chr10:625703..628425,2	MCF-7	breast:
11	chr10:593295..596957-chr10:620384..624822,4	MCF-7	breast:
12	chr10:599406..601960-chr10:605576..607787,2	MCF-7	breast:
13	chr10:625995..627810-chr10:664687..667494,2	K562	blood:
14	chr10:596736..599613-chr10:602463..604723,2	MCF-7	breast:
15	chr10:599406..601960-chr10:605576..607787,2	MCF-7	breast:
16	chr10:612084..613939-chr10:620156..623111,2	MCF-7	breast:
17	chr10:603209..605062-chr10:710188..713086,2	MCF-7	breast:
18	chr10:604798..606576-chr10:618326..620891,2	MCF-7	breast:
19	chr10:620907..622764-chr10:625703..628425,2	MCF-7	breast:
20	chr10:596736..599613-chr10:602463..604723,2	MCF-7	breast:
21	chr10:593219..595264-chr10:597541..599754,3	MCF-7	breast:
22	chr10:630264..632276-chr10:643488..645388,2	MCF-7	breast:
23	chr10:589190..591988-chr10:602233..604449,2	K562	blood:
24	chr10:593295..596957-chr10:620384..624822,4	MCF-7	breast:

No data

Variant related genes	Relation type
DIP2C	TF binding region
DIP2C	CpG island

Extended variants
information (count: 2350 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:2350 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs865289	chr10:595504-595505	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs187902063	chr10:595560-595561	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs535295426	chr10:595562-595563	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs555154039	chr10:595563-595564	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs572147698	chr10:595564-595565	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs534321510	chr10:595569-595570	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs557737445	chr10:595580-595581	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs1251342	chr10:595594-595595	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs544143419	chr10:595600-595601	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs139429573	chr10:595608-595609	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs574260818	chr10:595650-595651	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs543237760	chr10:595665-595666	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs11253136	chr10:595674-595675	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs59999413	chr10:595681-595682	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs374936093	chr10:595718-595719	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs78030666	chr10:595719-595720	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs367790664	chr10:595738-595739	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs117408151	chr10:595749-595750	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs533032590	chr10:595762-595763	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs549645046	chr10:595768-595769	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs191142894	chr10:595831-595832	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs79946723	chr10:595870-595871	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs144384598	chr10:595873-595874	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs60820926	chr10:595876-595877	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs7914425	chr10:595877-595878	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs7905658	chr10:595943-595944	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs145244782	chr10:595946-595947	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs11461177	chr10:595947-595948	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs184773326	chr10:595958-595959	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs557433672	chr10:595961-595962	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs376758398	chr10:595993-595994	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs369273748	chr10:596036-596037	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs537067199	chr10:596057-596058	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs7917823	chr10:596093-596094	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs142405596	chr10:596136-596137	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs189429844	chr10:596156-596157	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs181832753	chr10:596164-596165	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs7917949	chr10:596170-596171	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs573225226	chr10:596175-596176	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs139636856	chr10:596181-596182	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs565069358	chr10:596186-596187	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs530799085	chr10:596196-596197	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs185453772	chr10:596197-596198	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs550602086	chr10:596245-596246	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs144270232	chr10:596256-596257	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs529192218	chr10:596318-596319	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs374089198	chr10:596426-596427	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs149731580	chr10:596490-596491	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs548863395	chr10:596498-596499	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs559331745	chr10:596569-596570	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:54)

Disease	PMID	Source
Cancer	20164920	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	20409316	CNVD
Gastric adenocarcinoma	19115996	CNVD
Pilocytic astrocytoma	18622384	CNVD
Pilomyxoid astrocytoma	18622384	CNVD
Breast cancer	17133270	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Cancer	21129771	CNVD
Sudden cardiac death	19188705	CNVD
Digeorge syndrome	22283845	CNVD
Colorectal cancer	20709793	CNVD
Wilms tumour	19047088	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Barakat syndrome	22470819	CNVD
Melanoma	18172304	CNVD
Ovarian cancer	21720365	CNVD
Autism	18414403	CNVD
Malignant melanoma	18718029	CNVD
Breast cancer	22032731	CNVD
Medulloblastoma	16783165	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Phyllodes tumor	17334353	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Melanoma	17363583	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Breast cancer	21785460	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	21509527	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21525872	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21858162	CNVD
Obesity	19966786	CNVD

Chromatin state (count:1055 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:583200-604800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr10:590600-596000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr10:591200-595600	Enhancers	Placenta	Placenta
4	chr10:591400-595600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr10:592400-596000	Enhancers	Brain Anterior Caudate	brain
6	chr10:592600-595600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr10:592600-595600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
8	chr10:592800-595600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr10:592800-596200	Enhancers	Brain Cingulate Gyrus	brain
10	chr10:592800-596200	Enhancers	Brain Inferior Temporal Lobe	brain
11	chr10:593000-595600	Enhancers	Left Ventricle	heart
12	chr10:593000-596000	Enhancers	Fetal Brain Male	brain
13	chr10:593400-596400	Weak transcription	Duodenum Smooth Muscle	Duodenum
14	chr10:593600-596000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr10:593600-602800	Weak transcription	Fetal Intestine Small	intestine
16	chr10:593600-605000	Weak transcription	NH-A	brain
17	chr10:593800-597800	Weak transcription	Fetal Kidney	kidney
18	chr10:593800-600600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr10:594000-596600	Weak transcription	Stomach Smooth Muscle	stomach
20	chr10:594000-596800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr10:594000-596800	Weak transcription	Esophagus	oesophagus
22	chr10:594000-596800	Weak transcription	Fetal Stomach	stomach
23	chr10:594000-596800	Weak transcription	Right Atrium	heart
24	chr10:594000-597200	Weak transcription	Fetal Muscle Leg	muscle
25	chr10:594000-597400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
26	chr10:594000-597400	Weak transcription	Brain Substantia Nigra	brain
27	chr10:594000-601400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
28	chr10:594000-601800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr10:594000-604000	Weak transcription	Cortex derived primary cultured neurospheres	brain
30	chr10:594200-597800	Weak transcription	Fetal Brain Female	brain
31	chr10:594200-602800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr10:594200-604000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr10:594600-596200	Weak transcription	Pancreas	Pancrea
34	chr10:594600-599000	Weak transcription	Lung	lung
35	chr10:594600-600400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr10:594600-601600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr10:594600-604000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr10:594600-604000	Weak transcription	Brain Germinal Matrix	brain
39	chr10:594800-596600	Weak transcription	Skeletal Muscle Female	skeletal muscle
40	chr10:594800-597600	Weak transcription	Skeletal Muscle Male	skeletal muscle
41	chr10:595000-596000	Enhancers	Ovary	ovary
42	chr10:595200-595600	Enhancers	Psoas Muscle	Psoas
43	chr10:595200-595800	Enhancers	Spleen	Spleen
44	chr10:595200-597600	Enhancers	Colon Smooth Muscle	Colon
45	chr10:595200-602800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
46	chr10:595400-595600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr10:595400-595600	Enhancers	Fetal Muscle Trunk	muscle
48	chr10:595400-596000	Enhancers	Right Ventricle	heart
49	chr10:595400-596800	Weak transcription	Brain Angular Gyrus	brain
50	chr10:595400-597000	Weak transcription	Brain Hippocampus Middle	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links