Variant report

Variant	nsv948185
Chromosome Location	chr10:112693659-112697045
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:34)
CpG islands
(count:122)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:34 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr10:112696924-112696973	MCF-7	breast:	n/a	n/a
2	CTCF	chr10:112696883-112696918	MCF-7	breast:	n/a	n/a
3	CTCF	chr10:112696760-112697023	K562	blood:	n/a	n/a
4	CTCF	chr10:112696884-112696986	A549	lung:	n/a	n/a
5	CTCF	chr10:112696907-112696953	MCF-7	breast:	n/a	n/a
6	CTCF	chr10:112696677-112697035	A549	lung:	n/a	n/a
7	CTCF	chr10:112696906-112696964	K562	blood:	n/a	n/a
8	CTCF	chr10:112696809-112697003	A549	lung:	n/a	n/a
9	CTCF	chr10:112696877-112696987	MCF-7	breast:	n/a	n/a
10	CTCF	chr10:112696879-112696977	MCF-7	breast:	n/a	n/a
11	CTCF	chr10:112696877-112696982	GM12891	blood:	n/a	n/a
12	POLR2A	chr10:112696673-112696793	A549	lung:	n/a	n/a
13	POLR2A	chr10:112696799-112697063	Hela-S3	cervix:	n/a	n/a
14	POLR2A	chr10:112696656-112696664	A549	lung:	n/a	n/a
15	POLR2A	chr10:112696312-112696683	H1-hESC	embryonic stem cell:	n/a	n/a
16	POLR2A	chr10:112696650-112696725	A549	lung:	n/a	n/a
17	POLR2A	chr10:112696918-112697091	K562	blood:	n/a	n/a
18	POLR2A	chr10:112696241-112697098	GM12892	blood:	n/a	n/a
19	POLR2A	chr10:112696306-112696490	H1-hESC	embryonic stem cell:	n/a	n/a
20	POLR2A	chr10:112696536-112696650	A549	lung:	n/a	n/a
21	POLR2A	chr10:112696292-112696702	Hela-S3	cervix:	n/a	n/a
22	POLR2A	chr10:112696807-112696815	A549	lung:	n/a	n/a
23	POLR2A	chr10:112696816-112696976	A549	lung:	n/a	n/a
24	POLR2A	chr10:112696193-112697139	GM12878	blood:	n/a	n/a
25	POLR2A	chr10:112694665-112694840	K562	blood:	n/a	n/a
26	POLR2A	chr10:112696298-112696439	Hela-S3	cervix:	n/a	n/a
27	POLR2A	chr10:112696697-112696984	GM12878	blood:	n/a	n/a
28	POLR2A	chr10:112696816-112696820	A549	lung:	n/a	n/a
29	POLR2A	chr10:112696360-112697140	GM12892	blood:	n/a	n/a
30	POLR2A	chr10:112696797-112696995	H1-hESC	embryonic stem cell:	n/a	n/a
31	ZBTB33	chr10:112696700-112697057	K562	blood:	n/a	n/a
32	ZBTB33	chr10:112696270-112696646	K562	blood:	n/a	n/a
33	ZNF384	chr10:112696432-112696447	GM12878	blood:	n/a	n/a
34	ZNF384	chr10:112696311-112696409	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:112696816-112696866	U87	brain:	n/a
2	chr10:112696816-112696866	GM12878	blood:	n/a
3	chr10:112696816-112696866	AG09309	skin:	n/a
4	chr10:112696816-112696866	GM12892	blood:	n/a
5	chr10:112696816-112696866	PANC-1	pancreas:	n/a
6	chr10:112696786-112696836	HRCEpiC	kidney:	n/a
7	chr10:112696786-112696836	PANC-1	pancreas:	n/a
8	chr10:112696816-112696866	NHDF-neo	bronchial:	n/a
9	chr10:112696786-112696836	BE2_C	brain:	n/a
10	chr10:112696786-112696836	HCM	heart:	n/a
11	chr10:112696816-112696866	MCF10A-Er-Src	breast:	n/a
12	chr10:112696786-112696836	HIPEpiC	eye:	n/a
13	chr10:112696816-112696866	GM06990	blood:	n/a
14	chr10:112696786-112696836	AG04450	lung:	fetal
15	chr10:112696786-112696836	LNCaP	prostate:	n/a
16	chr10:112696786-112696836	HNPCEpiC	eye:	n/a
17	chr10:112696786-112696836	SAEC	small airway:	n/a
18	chr10:112696816-112696866	Caco-2	colon:	n/a
19	chr10:112696816-112696866	SK-N-SH_RA	brain:	n/a
20	chr10:112696816-112696866	HIPEpiC	eye:	n/a
21	chr10:112696816-112696866	SKMC	muscle:	n/a
22	chr10:112696816-112696866	ovcar-3	ovarian:	n/a
23	chr10:112696816-112696866	AG04450	lung:	fetal
24	chr10:112696786-112696836	Jurkat	blood:	n/a
25	chr10:112696816-112696866	NHBE	bronchial:	n/a
26	chr10:112696816-112696866	MCF-7	breast:	n/a
27	chr10:112696816-112696866	AG09319	gingival:	n/a
28	chr10:112696816-112696866	Hela-S3	cervix:	n/a
29	chr10:112696816-112696866	HRE	kidney:	n/a
30	chr10:112696786-112696836	GM12892	blood:	n/a
31	chr10:112696816-112696866	Hepatocyte	liver:	n/a
32	chr10:112696786-112696836	HEEpiC	esophagus:	n/a
33	chr10:112696786-112696836	Hela-S3	cervix:	n/a
34	chr10:112696816-112696866	AG04449	skin:	fetal
35	chr10:112696786-112696836	NB4	blood:	n/a
36	chr10:112696786-112696836	Hepatocyte	liver:	n/a
37	chr10:112696786-112696836	Caco-2	colon:	n/a
38	chr10:112696816-112696866	Jurkat	blood:	n/a
39	chr10:112696786-112696836	ovcar-3	ovarian:	n/a
40	chr10:112696816-112696866	HCF	heart:	n/a
41	chr10:112696786-112696836	GM12891	blood:	n/a
42	chr10:112696786-112696836	IMR90	lung:	fetal
43	chr10:112696786-112696836	HPAEpiC	pulmonary alveolar:	n/a
44	chr10:112696786-112696836	AG09309	skin:	n/a
45	chr10:112696816-112696866	RPTEC	kidney:	n/a
46	chr10:112696786-112696836	HAEpiC	amniotic membrane:	n/a
47	chr10:112696786-112696836	AG09319	gingival:	n/a
48	chr10:112696786-112696836	HUVEC	blood vessel:	n/a
49	chr10:112696816-112696866	LNCaP	prostate:	n/a
50	chr10:112696816-112696866	HL-60	blood:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:112691219..112695362-chr10:112695848..112700041,5	MCF-7	breast:
2	chr10:112677742..112679922-chr10:112696330..112699215,3	K562	blood:
3	chr10:112677485..112680905-chr10:112696350..112700143,5	K562	blood:
4	chr10:112693592..112695425-chr10:112736222..112738778,2	MCF-7	breast:
5	chr10:112691670..112694592-chr10:112699465..112702013,2	K562	blood:

No data

Variant related genes	Relation type
RPL13AP6	TF binding region
RPL13AP6	CpG island
ENSG00000234118	chromatin interactions
ENSG00000214413	chromatin interactions
ENSG00000108061	chromatin interactions

Extended variants
information (count: 132 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:132 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs549476738	chr10:112693667-112693668	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs529966781	chr10:112693673-112693674	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs548123441	chr10:112693688-112693689	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs527777672	chr10:112693704-112693705	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs139811077	chr10:112693709-112693710	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs143207552	chr10:112693717-112693718	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs571562119	chr10:112693779-112693780	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs368050206	chr10:112693806-112693807	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs187047175	chr10:112693826-112693827	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs554040125	chr10:112693910-112693911	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs4918613	chr10:112694030-112694031	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs536476908	chr10:112694035-112694036	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs555488293	chr10:112694066-112694067	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs573818622	chr10:112694080-112694081	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs544220628	chr10:112694094-112694095	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs146750426	chr10:112694104-112694105	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs556196357	chr10:112694110-112694111	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs191553365	chr10:112694124-112694125	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs183708259	chr10:112694125-112694126	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs560059755	chr10:112694206-112694207	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs370768901	chr10:112694268-112694269	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs187988414	chr10:112694269-112694270	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs561044247	chr10:112694276-112694277	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs140380394	chr10:112694309-112694310	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs192262090	chr10:112694316-112694317	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs1571240	chr10:112694342-112694343	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs552350104	chr10:112694407-112694408	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs145578826	chr10:112694417-112694418	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs548049569	chr10:112694420-112694421	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs566281857	chr10:112694615-112694616	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs111999450	chr10:112694640-112694641	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs571038690	chr10:112694681-112694682	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs367893040	chr10:112694714-112694715	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs185842610	chr10:112694722-112694723	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs555246840	chr10:112694731-112694732	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs535259090	chr10:112694811-112694812	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs531709273	chr10:112694858-112694859	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs150973382	chr10:112694883-112694884	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs534681075	chr10:112694898-112694899	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs550510998	chr10:112694903-112694904	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs553303586	chr10:112695017-112695018	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs140833246	chr10:112695025-112695026	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs538282355	chr10:112695026-112695027	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs112152302	chr10:112695030-112695031	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs572291141	chr10:112695059-112695060	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs542367097	chr10:112695215-112695216	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs560758552	chr10:112695264-112695265	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs568321113	chr10:112695272-112695273	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs543533604	chr10:112695316-112695317	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs575045856	chr10:112695364-112695365	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:74)

Disease	PMID	Source
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	20729466	CNVD
Paraganglioma	17535989	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Pulmonary chondroma	17535989	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	17387387	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	16573809	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	16608533	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Myxofibrosarcoma	16751306	CNVD
Cornelia de Lange syndrome	24599119	CNVD
T-cell lymphomas	19863542	CNVD
Breast cancer	16397240	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	16616336	CNVD
Chronic lymphocytic leukemia	18645599	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	21509527	CNVD
Barrett''s syndrome	19417022	CNVD
Sezary syndrome	18413736	CNVD
Cornelia de Lange syndrome	21085971	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:145 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:112680600-112696600	Weak transcription	Lung	lung
2	chr10:112680600-112706800	Weak transcription	Esophagus	oesophagus
3	chr10:112680800-112704600	Weak transcription	Aorta	Aorta
4	chr10:112681000-112696400	Weak transcription	Fetal Stomach	stomach
5	chr10:112681000-112696600	Weak transcription	Thymus	Thymus
6	chr10:112681000-112704600	Weak transcription	Right Ventricle	heart
7	chr10:112682000-112700600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr10:112682000-112702000	Weak transcription	Cortex derived primary cultured neurospheres	brain
9	chr10:112682000-112702200	Weak transcription	Brain Germinal Matrix	brain
10	chr10:112682000-112704600	Weak transcription	Brain Hippocampus Middle	brain
11	chr10:112682000-112708400	Weak transcription	Primary monocytes fromperipheralblood	blood
12	chr10:112682000-112732400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
13	chr10:112683000-112700800	Weak transcription	Dnd41	blood
14	chr10:112683200-112694000	Enhancers	Primary T helper cells PMA-I stimulated	--
15	chr10:112684200-112696400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr10:112684200-112700800	Weak transcription	Primary hematopoietic stem cells	blood
17	chr10:112684200-112701000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr10:112684400-112696600	Weak transcription	Rectal Mucosa Donor 29	rectum
19	chr10:112684400-112712600	Weak transcription	HepG2	liver
20	chr10:112684800-112696400	Weak transcription	Spleen	Spleen
21	chr10:112685200-112719200	Weak transcription	A549	lung
22	chr10:112685600-112695800	Weak transcription	Fetal Intestine Small	intestine
23	chr10:112687600-112697800	Weak transcription	Pancreatic Islets	Pancreatic Islet
24	chr10:112688200-112696800	Weak transcription	Primary neutrophils fromperipheralblood	blood
25	chr10:112688600-112696000	Weak transcription	Primary T cells fromperipheralblood	blood
26	chr10:112688600-112696400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr10:112688600-112696600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
28	chr10:112688600-112697000	Weak transcription	Fetal Brain Female	brain
29	chr10:112689200-112697200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
30	chr10:112689400-112704600	Weak transcription	Left Ventricle	heart
31	chr10:112689600-112701600	Weak transcription	Primary B cells from cord blood	blood
32	chr10:112689600-112714400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chr10:112689800-112702200	Weak transcription	Primary T cells from cord blood	blood
34	chr10:112690200-112707800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
35	chr10:112690800-112702200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr10:112691200-112696400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
37	chr10:112691200-112700400	Weak transcription	Monocytes-CD14+_RO01746	blood
38	chr10:112691600-112696600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
39	chr10:112691800-112703600	Weak transcription	Rectal Smooth Muscle	rectum
40	chr10:112692000-112696400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr10:112692000-112700800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr10:112692000-112703200	Weak transcription	Liver	Liver
43	chr10:112692000-112722000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
44	chr10:112692200-112694800	Weak transcription	GM12878-XiMat	blood
45	chr10:112692400-112693800	Weak transcription	Colon Smooth Muscle	Colon
46	chr10:112692400-112696200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr10:112692400-112696800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
48	chr10:112692400-112700400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr10:112692400-112701200	Weak transcription	Rectal Mucosa Donor 31	rectum
50	chr10:112692400-112703600	Weak transcription	NHLF	lung

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