Variant report

Variant	nsv6377
Chromosome Location	chr8:126579620-126639253
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:143)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:143 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr8:126606536..126608218-chr8:126626974..126628718,2	MCF-7	breast:
2	chr8:126619524..126621490-chr8:126626488..126629333,2	K562	blood:
3	chr8:126458069..126459913-chr8:126608765..126611679,2	MCF-7	breast:
4	chr8:126453555..126455063-chr8:126584275..126586099,2	MCF-7	breast:
5	chr8:126585008..126593535-chr8:126599853..126611131,18	MCF-7	breast:
6	chr8:126586635..126589036-chr8:126593188..126594968,2	MCF-7	breast:
7	chr8:126586635..126589036-chr8:126593188..126594968,2	MCF-7	breast:
8	chr8:126593358..126595719-chr8:126599796..126603386,4	K562	blood:
9	chr8:126619990..126624184-chr8:126625667..126627988,3	K562	blood:
10	chr8:126605765..126606903-chr8:126656478..126657365,5	MCF-7	breast:
11	chr8:126442285..126445207-chr8:126590362..126592465,3	MCF-7	breast:
12	chr8:126610735..126612592-chr8:126617138..126620158,3	MCF-7	breast:
13	chr8:126590849..126591449-chr8:126602043..126602895,2	MCF-7	breast:
14	chr8:126570042..126574536-chr8:126578331..126584724,7	MCF-7	breast:
15	chr8:126610735..126612592-chr8:126617138..126620158,3	MCF-7	breast:
16	chr8:126615487..126618123-chr8:126620210..126621932,2	K562	blood:
17	chr8:126442729..126444290-chr8:126611048..126613106,2	MCF-7	breast:
18	chr8:126608438..126611381-chr8:126617335..126619462,2	K562	blood:
19	chr8:126558356..126560291-chr8:126608744..126610330,2	MCF-7	breast:
20	chr8:126602067..126602597-chr8:126618483..126619059,2	MCF-7	breast:
21	chr8:126623702..126626459-chr8:126629825..126632775,2	K562	blood:
22	chr8:126442143..126446665-chr8:126589959..126594389,6	MCF-7	breast:
23	chr8:126449216..126452088-chr8:126604011..126606730,3	MCF-7	breast:
24	chr8:126601003..126603272-chr8:126603536..126606567,4	MCF-7	breast:
25	chr8:126551415..126553791-chr8:126604012..126607735,3	MCF-7	breast:
26	chr8:126584493..126586027-chr8:126604796..126607336,2	MCF-7	breast:
27	chr8:125984215..125987175-chr8:126588399..126591130,2	MCF-7	breast:
28	chr8:126592991..126596537-chr8:126599819..126603670,10	MCF-7	breast:
29	chr8:126589816..126592471-chr8:126605971..126608086,2	MCF-7	breast:
30	chr8:126445273..126447091-chr8:126638260..126639894,2	MCF-7	breast:
31	chr8:126441094..126445421-chr8:126601055..126606149,10	MCF-7	breast:
32	chr8:126588355..126592631-chr8:126600736..126604091,3	MCF-7	breast:
33	chr8:126636675..126638535-chr8:126641760..126643803,2	MCF-7	breast:
34	chr8:126601013..126605207-chr8:126607092..126609721,3	MCF-7	breast:
35	chr8:126615487..126618123-chr8:126620210..126621932,2	K562	blood:
36	chr8:126602958..126605776-chr8:126609153..126611231,2	MCF-7	breast:
37	chr8:126618476..126621676-chr8:126622245..126624732,3	MCF-7	breast:
38	chr8:126628692..126630549-chr8:126631785..126633599,2	MCF-7	breast:
39	chr8:126602958..126605776-chr8:126609153..126611231,2	MCF-7	breast:
40	chr8:126624246..126627028-chr8:126627335..126628862,2	MCF-7	breast:
41	chr8:126541134..126543956-chr8:126578428..126580146,2	MCF-7	breast:
42	chr8:126620542..126623199-chr8:126642002..126644865,2	MCF-7	breast:
43	chr8:126585008..126593535-chr8:126599853..126611131,18	MCF-7	breast:
44	chr8:126602321..126604094-chr8:126616027..126618273,2	MCF-7	breast:
45	chr8:126606627..126608562-chr8:126611107..126612785,3	MCF-7	breast:
46	chr8:126242654..126243238-chr8:126601971..126602543,2	MCF-7	breast:
47	chr8:126634124..126636171-chr8:126637247..126639701,2	MCF-7	breast:
48	chr8:126442074..126444761-chr8:126614097..126617217,3	MCF-7	breast:
49	chr8:126441876..126443821-chr8:126595052..126596590,2	MCF-7	breast:
50	chr8:126442492..126444588-chr8:126626090..126628440,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TRIB1-12	chr8:126625712-126626709	NONHSAT128977
2	lnc-TRIB1-12	chr8:126626798-126627375	NONHSAT128977

No data

Variant related genes	Relation type
ENSG00000180938	chromatin interactions
ENSG00000156831	chromatin interactions
ENSG00000266452	chromatin interactions
ENSG00000164961	chromatin interactions
ENSG00000173334	chromatin interactions

Extended variants
information (count: 2079 )
Associated
traits (count: 141 )

Variant overlapped rSNPs/rCNVs (count:2079 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs149303278	chr8:126579647-126579648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs532985228	chr8:126579652-126579653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs552610610	chr8:126579775-126579776	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs559607607	chr8:126579786-126579787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs73350810	chr8:126579882-126579883	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs540030393	chr8:126579911-126579912	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs548206883	chr8:126579920-126579921	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs568411781	chr8:126579933-126579934	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs537389154	chr8:126580027-126580028	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs536146726	chr8:126580030-126580031	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs551002297	chr8:126580094-126580095	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs144575504	chr8:126580113-126580114	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs539669509	chr8:126580162-126580163	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs558437218	chr8:126580172-126580173	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs148062405	chr8:126580173-126580174	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs573000631	chr8:126580226-126580227	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs535438234	chr8:126580248-126580249	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs374460820	chr8:126580298-126580299	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs188379960	chr8:126580322-126580323	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs544447960	chr8:126580364-126580365	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs555700442	chr8:126580380-126580381	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs193027739	chr8:126580421-126580422	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs577731787	chr8:126580447-126580448	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs112138191	chr8:126580462-126580463	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs540087611	chr8:126580503-126580504	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs182997851	chr8:126580573-126580574	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs559777428	chr8:126580605-126580606	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs897149	chr8:126580618-126580619	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs548168144	chr8:126580620-126580621	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs187338243	chr8:126580667-126580668	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs530819696	chr8:126580695-126580696	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs191701306	chr8:126580697-126580698	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs571075341	chr8:126580702-126580703	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs75536983	chr8:126580722-126580723	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs2219142	chr8:126580797-126580798	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs564411936	chr8:126580828-126580829	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs369741583	chr8:126580848-126580849	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs72722698	chr8:126580855-126580856	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs566560857	chr8:126580992-126580993	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs535499460	chr8:126581014-126581015	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs75066746	chr8:126581071-126581072	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs577760179	chr8:126581081-126581082	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs375291338	chr8:126581085-126581086	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs568841707	chr8:126581103-126581104	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs75154631	chr8:126581120-126581121	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs142339727	chr8:126581130-126581131	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs145952514	chr8:126581131-126581132	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs540420437	chr8:126581141-126581142	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs75154689	chr8:126581144-126581145	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs897148	chr8:126581168-126581169	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

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:976 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:126569200-126580200	Weak transcription	Left Ventricle	heart
2	chr8:126569800-126588200	Weak transcription	Spleen	Spleen
3	chr8:126572600-126581200	Weak transcription	HMEC	breast
4	chr8:126575400-126580200	Weak transcription	Skeletal Muscle Male	skeletal muscle
5	chr8:126575400-126580400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr8:126576200-126581200	Weak transcription	NHDF-Ad	bronchial
7	chr8:126576400-126580400	Weak transcription	Adipose Nuclei	Adipose
8	chr8:126576400-126580400	Weak transcription	Right Atrium	heart
9	chr8:126576400-126581600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr8:126576400-126581800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr8:126578800-126582400	Weak transcription	Sigmoid Colon	Sigmoid Colon
12	chr8:126578800-126583800	Weak transcription	Rectal Mucosa Donor 31	rectum
13	chr8:126578800-126586600	Weak transcription	Liver	Liver
14	chr8:126579800-126583000	Enhancers	Fetal Lung	lung
15	chr8:126580000-126583000	Enhancers	Stomach Smooth Muscle	stomach
16	chr8:126580200-126580400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr8:126580200-126580600	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr8:126580200-126580600	Enhancers	Psoas Muscle	Psoas
19	chr8:126580200-126580800	Enhancers	Skeletal Muscle Female	skeletal muscle
20	chr8:126580200-126581000	Enhancers	Fetal Brain Male	brain
21	chr8:126580200-126581200	Enhancers	Left Ventricle	heart
22	chr8:126580200-126582400	Enhancers	Colon Smooth Muscle	Colon
23	chr8:126580200-126582800	Enhancers	Skeletal Muscle Male	skeletal muscle
24	chr8:126580200-126583000	Enhancers	Fetal Muscle Leg	muscle
25	chr8:126580200-126583000	Enhancers	Fetal Stomach	stomach
26	chr8:126580400-126580600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
27	chr8:126580400-126580600	Enhancers	Fetal Muscle Trunk	muscle
28	chr8:126580400-126580600	Enhancers	Fetal Thymus	thymus
29	chr8:126580400-126581400	Enhancers	GM12878-XiMat	blood
30	chr8:126580400-126581600	Enhancers	Primary neutrophils fromperipheralblood	blood
31	chr8:126580400-126581600	Enhancers	Lung	lung
32	chr8:126580400-126581800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr8:126580400-126581800	Enhancers	Primary B cells from peripheral blood	blood
34	chr8:126580400-126582200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr8:126580400-126582200	Enhancers	Adipose Nuclei	Adipose
36	chr8:126580400-126582600	Enhancers	Right Atrium	heart
37	chr8:126580400-126582800	Enhancers	Ovary	ovary
38	chr8:126580400-126583000	Enhancers	Colonic Mucosa	Colon
39	chr8:126580600-126581600	Enhancers	Primary B cells from cord blood	blood
40	chr8:126580600-126581600	Weak transcription	Fetal Muscle Trunk	muscle
41	chr8:126580600-126581600	Weak transcription	Psoas Muscle	Psoas
42	chr8:126580600-126581800	Weak transcription	Fetal Thymus	thymus
43	chr8:126580800-126581000	Enhancers	Duodenum Mucosa	Duodenum
44	chr8:126580800-126581200	Weak transcription	Skeletal Muscle Female	skeletal muscle
45	chr8:126581000-126583000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr8:126581000-126583800	Weak transcription	Duodenum Mucosa	Duodenum
47	chr8:126581200-126581600	Weak transcription	Left Ventricle	heart
48	chr8:126581200-126581800	Enhancers	Osteobl	bone
49	chr8:126581200-126582200	Enhancers	NHDF-Ad	bronchial
50	chr8:126581200-126583000	Enhancers	Skeletal Muscle Female	skeletal muscle

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links