Variant report

Variant	nsv1015513
Chromosome Location	chr8:126602536-126618074
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:62)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:62 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:126442729..126444290-chr8:126611048..126613106,2	MCF-7	breast:
2	chr8:126608438..126611381-chr8:126617335..126619462,2	K562	blood:
3	chr8:126590849..126591449-chr8:126602043..126602895,2	MCF-7	breast:
4	chr8:126602321..126604094-chr8:126616027..126618273,2	MCF-7	breast:
5	chr8:126520525..126522060-chr8:126604216..126606404,2	MCF-7	breast:
6	chr8:126593358..126595719-chr8:126599796..126603386,4	K562	blood:
7	chr8:126601013..126605207-chr8:126607092..126609721,3	MCF-7	breast:
8	chr8:126606536..126608218-chr8:126626974..126628718,2	MCF-7	breast:
9	chr8:126593642..126596532-chr8:126599701..126606279,16	MCF-7	breast:
10	chr8:126608438..126611381-chr8:126617335..126619462,2	K562	blood:
11	chr11:2133266..2133781-chr8:126607043..126607813,2	HCT-116	colon:
12	chr8:126551415..126553791-chr8:126604012..126607735,3	MCF-7	breast:
13	chr8:126601003..126603272-chr8:126603536..126606567,4	MCF-7	breast:
14	chr8:126440732..126445779-chr8:126600349..126612045,20	MCF-7	breast:
15	chr8:126585008..126593535-chr8:126599853..126611131,18	MCF-7	breast:
16	chr8:126520498..126522119-chr8:126613658..126615873,2	MCF-7	breast:
17	chr8:126441405..126444224-chr8:126614301..126619460,8	MCF-7	breast:
18	chr8:126602067..126602597-chr8:126618483..126619059,2	MCF-7	breast:
19	chr8:126440111..126444206-chr8:126606253..126610724,8	MCF-7	breast:
20	chr8:126455135..126457376-chr8:126604842..126607089,2	MCF-7	breast:
21	chr8:126602958..126605776-chr8:126609153..126611231,2	MCF-7	breast:
22	chr8:126610481..126612816-chr8:126612922..126614971,2	MCF-7	breast:
23	chr8:126507152..126508926-chr8:126605095..126607004,2	MCF-7	breast:
24	chr8:126458069..126459913-chr8:126608765..126611679,2	MCF-7	breast:
25	chr8:126612687..126615177-chr8:126616929..126619166,2	MCF-7	breast:
26	chr8:126605765..126606903-chr8:126656478..126657365,5	MCF-7	breast:
27	chr8:126593622..126595846-chr8:126610575..126612204,2	MCF-7	breast:
28	chr8:126602958..126605776-chr8:126609153..126611231,2	MCF-7	breast:
29	chr8:126442074..126444761-chr8:126614097..126617217,3	MCF-7	breast:
30	chr8:126614837..126616782-chr8:126623338..126626219,3	MCF-7	breast:
31	chr8:126443894..126444669-chr8:126605677..126606770,5	MCF-7	breast:
32	chr8:126588355..126592631-chr8:126600736..126604091,3	MCF-7	breast:
33	chr8:126615487..126618123-chr8:126620210..126621932,2	K562	blood:
34	chr8:126605005..126607033-chr8:126613419..126615572,2	MCF-7	breast:
35	chr8:126610735..126612592-chr8:126617138..126620158,3	MCF-7	breast:
36	chr8:126589816..126592471-chr8:126605971..126608086,2	MCF-7	breast:
37	chr8:126610735..126612592-chr8:126617138..126620158,3	MCF-7	breast:
38	chr8:126591683..126594528-chr8:126604953..126606548,2	K562	blood:
39	chr8:126592961..126594666-chr8:126603938..126605486,2	MCF-7	breast:
40	chr8:126601013..126605207-chr8:126607092..126609721,3	MCF-7	breast:
41	chr8:126606627..126608562-chr8:126611107..126612785,3	MCF-7	breast:
42	chr8:126443986..126444706-chr8:126602365..126602966,2	MCF-7	breast:
43	chr8:126290887..126293286-chr8:126610271..126611815,2	K562	blood:
44	chr8:126610315..126613289-chr8:126653712..126655623,2	MCF-7	breast:
45	chr8:126605898..126607935-chr8:126618594..126621504,4	MCF-7	breast:
46	chr8:126584493..126586027-chr8:126604796..126607336,2	MCF-7	breast:
47	chr8:126550463..126552355-chr8:126601119..126603239,2	MCF-7	breast:
48	chr8:126612687..126615177-chr8:126616929..126619166,2	MCF-7	breast:
49	chr8:126509004..126511702-chr8:126604698..126606294,2	MCF-7	breast:
50	chr8:126616447..126617973-chr8:126621582..126623418,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000173334	chromatin interactions
ENSG00000266452	chromatin interactions

Extended variants
information (count: 611 )
Associated
traits (count: 141 )

Variant overlapped rSNPs/rCNVs (count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs571678124	chr8:126602546-126602547	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs534472946	chr8:126602582-126602583	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs189609580	chr8:126602598-126602599	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs201965919	chr8:126602620-126602621	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs536478961	chr8:126602627-126602628	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs571485576	chr8:126602629-126602630	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs575778521	chr8:126602649-126602650	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs544704388	chr8:126602739-126602740	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs538509403	chr8:126602756-126602757	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs181975131	chr8:126602885-126602886	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs34813925	chr8:126602888-126602889	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs117001382	chr8:126602919-126602920	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs541298315	chr8:126602943-126602944	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs34074756	chr8:126602992-126602993	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs529891847	chr8:126603133-126603134	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs145821821	chr8:126603186-126603187	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs4870946	chr8:126603194-126603195	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs369984747	chr8:126603195-126603196	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs531799052	chr8:126603212-126603213	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs60501655	chr8:126603283-126603284	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs200367925	chr8:126603284-126603285	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs138731226	chr8:126603314-126603315	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs117536507	chr8:126603319-126603320	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs4871618	chr8:126603334-126603335	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs548053382	chr8:126603340-126603341	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs187067993	chr8:126603351-126603352	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs143982914	chr8:126603380-126603381	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs10110589	chr8:126603390-126603391	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs147311054	chr8:126603451-126603452	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs533375210	chr8:126603481-126603482	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs369324311	chr8:126603483-126603484	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs538310466	chr8:126603493-126603494	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs558250571	chr8:126603516-126603517	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs571994713	chr8:126603517-126603518	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs368647132	chr8:126603526-126603527	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs374550420	chr8:126603534-126603535	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs554848740	chr8:126603565-126603566	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs189793364	chr8:126603573-126603574	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs181396832	chr8:126603580-126603581	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs185623444	chr8:126603590-126603591	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs190087414	chr8:126603591-126603592	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs545497274	chr8:126603594-126603595	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs182286060	chr8:126603623-126603624	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs113844043	chr8:126603688-126603689	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs33997582	chr8:126603697-126603698	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs527675702	chr8:126603717-126603718	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs36111824	chr8:126603721-126603722	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs10111011	chr8:126603725-126603726	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs567653236	chr8:126603730-126603731	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs149439322	chr8:126603746-126603747	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:141)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	17603634	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	20729466	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Developmental delay	21147756	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	20932292	CNVD
Gastric cancer	22539939	CNVD
Breast cancer	22056952	CNVD
Langer-Giedion syndrome	16773131	CNVD
Lung cancer	16740712	CNVD
Mental retardation	16773131	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Langer-Giedion syndrome	22470819	CNVD
Cornelia de Lange syndrome	24599119	CNVD
Gastric cancer	21528007	CNVD
Breast cancer	22532251	CNVD
Cervical cancer	21062161	CNVD
Cancer	21129771	CNVD
benign familial neonatal convulsions	18472482	CNVD
Breast cancer	16417655	CNVD
Astrocytoma	17387387	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
T-cell lymphomas	19863542	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	20607354	CNVD
Breast cancer	20814816	CNVD
Colorectal cancer	22486879	CNVD
Breast cancer	17908964	CNVD
Colorectal cancer	20031965	CNVD
Hepatocellular carcinoma	16750200	CNVD
Ovarian cancer	17908964	CNVD
Ovarian cancer	20031965	CNVD
Prostate cancer	20031965	CNVD
Non-small cell lung cancer	17643093	CNVD
Prostate cancer	19242612	CNVD
Colorectal cancer	16774939	CNVD
Glioblastoma multiforme	18628472	CNVD
Malignant melanoma	17260012	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	16397240	CNVD
Multiple myeloma	16461302	CNVD
Multiple myeloma	16616336	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Breast cancer	21364760	CNVD
Burkitt''s lymphoma	20823134	CNVD
Colorectal cancer	21645411	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Acute myeloid leukemia	17268525	CNVD
Acute myeloid leukemia	18379011	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21611746	CNVD
Ductal carcinoma	22052326	CNVD
Gastric cancer	18160780	CNVD
Gastric cancer	21635755	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute lymphoblastic leukemia	21339820	CNVD

Chromatin state (count:345 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:126592600-126603800	Weak transcription	Pancreas	Pancrea
2	chr8:126600000-126604200	Weak transcription	Aorta	Aorta
3	chr8:126602000-126603000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr8:126602200-126603400	Enhancers	GM12878-XiMat	blood
5	chr8:126602200-126603600	Enhancers	Rectal Mucosa Donor 31	rectum
6	chr8:126602200-126604400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr8:126602200-126606600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr8:126602200-126608600	Enhancers	Placenta	Placenta
9	chr8:126602400-126602800	Enhancers	Primary B cells from peripheral blood	blood
10	chr8:126602400-126603000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr8:126602400-126606800	Enhancers	NHEK	skin
12	chr8:126602400-126607400	Weak transcription	Rectal Mucosa Donor 29	rectum
13	chr8:126602600-126605400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr8:126602600-126606800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr8:126602800-126603400	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr8:126602800-126603800	Enhancers	Placenta Amnion	Placenta Amnion
17	chr8:126602800-126607400	Weak transcription	Primary B cells from peripheral blood	blood
18	chr8:126603000-126603400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr8:126603200-126604200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr8:126603400-126604600	Enhancers	Fetal Intestine Small	intestine
21	chr8:126603400-126605400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr8:126603600-126603800	Enhancers	A549	lung
23	chr8:126603600-126604000	Weak transcription	Rectal Mucosa Donor 31	rectum
24	chr8:126603600-126605200	Enhancers	HMEC	breast
25	chr8:126603800-126604600	Weak transcription	Placenta Amnion	Placenta Amnion
26	chr8:126603800-126607000	Enhancers	Esophagus	oesophagus
27	chr8:126603800-126607200	Enhancers	Pancreas	Pancrea
28	chr8:126604000-126605600	Weak transcription	A549	lung
29	chr8:126604000-126605800	Enhancers	HSMMtube	muscle
30	chr8:126604000-126606200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
31	chr8:126604000-126608800	Enhancers	Rectal Mucosa Donor 31	rectum
32	chr8:126604200-126604600	Enhancers	Aorta	Aorta
33	chr8:126604200-126605200	Enhancers	Skeletal Muscle Male	skeletal muscle
34	chr8:126604200-126605600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr8:126604400-126604600	Enhancers	Left Ventricle	heart
36	chr8:126604400-126605000	Enhancers	Breast Myoepithelial Primary Cells	Breast
37	chr8:126604400-126605000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr8:126604400-126605200	Enhancers	Primary T cells fromperipheralblood	blood
39	chr8:126604600-126604800	Enhancers	Right Ventricle	heart
40	chr8:126604600-126605400	Weak transcription	Fetal Intestine Small	intestine
41	chr8:126604600-126606400	Weak transcription	Left Ventricle	heart
42	chr8:126604600-126607000	Enhancers	Placenta Amnion	Placenta Amnion
43	chr8:126604800-126606600	Weak transcription	Right Ventricle	heart
44	chr8:126605000-126605200	Enhancers	Lung	lung
45	chr8:126605000-126605200	Enhancers	Spleen	Spleen
46	chr8:126605000-126605800	Enhancers	Adipose Nuclei	Adipose
47	chr8:126605000-126606200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr8:126605000-126606600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
49	chr8:126605200-126605600	Enhancers	Fetal Thymus	thymus
50	chr8:126605200-126605800	Weak transcription	Lung	lung

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