Variant report

Variant	nsv968508
Chromosome Location	chr8:48924846-48957474
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:48954659-48955530	HepG2	liver:	n/a	n/a
2	BATF	chr8:48947286-48947520	GM12878	blood:	n/a	n/a
3	BATF	chr8:48947249-48947622	GM12878	blood:	n/a	n/a
4	BATF	chr8:48949938-48950269	GM12878	blood:	n/a	n/a
5	BHLHE40	chr8:48954895-48955210	HepG2	liver:	n/a	n/a
6	BHLHE40	chr8:48954919-48955131	HepG2	liver:	n/a	n/a
7	BHLHE40	chr8:48954910-48955174	HepG2	liver:	n/a	n/a
8	CEBPB	chr8:48933192-48933550	HepG2	liver:	n/a	n/a
9	CEBPB	chr8:48936296-48936443	HepG2	liver:	n/a	chr8:48936386-48936397
10	CEBPB	chr8:48936395-48936460	K562	blood:	n/a	n/a
11	CEBPB	chr8:48936299-48936499	HepG2	liver:	n/a	chr8:48936386-48936397
12	CEBPB	chr8:48933179-48933498	MCF-7	breast:	n/a	n/a
13	CEBPB	chr8:48933187-48933545	K562	blood:	n/a	n/a
14	CEBPB	chr8:48933199-48933523	A549	lung:	n/a	n/a
15	CEBPB	chr8:48932005-48932104	HepG2	liver:	n/a	chr8:48932039-48932050
16	CEBPB	chr8:48942774-48942932	K562	blood:	n/a	n/a
17	CEBPB	chr8:48933126-48933611	A549	lung:	n/a	n/a
18	CEBPB	chr8:48933209-48933470	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr8:48933246-48933523	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr8:48933206-48933548	IMR90	lung:	n/a	n/a
21	CEBPB	chr8:48933247-48933440	HepG2	liver:	n/a	n/a
22	CEBPB	chr8:48933238-48933571	ECC-1	luminal epithelium:	n/a	n/a
23	CEBPB	chr8:48947421-48947481	IMR90	lung:	n/a	n/a
24	CEBPB	chr8:48933174-48933540	A549	lung:	n/a	n/a
25	CTCF	chr8:48936540-48936690	AG04450	lung:	n/a	n/a
26	ELK1	chr8:48950094-48950140	GM12878	blood:	n/a	n/a
27	EP300	chr8:48954776-48955261	HepG2	liver:	n/a	chr8:48955089-48955103 chr8:48955031-48955041 chr8:48955093-48955107 chr8:48955094-48955108
28	EP300	chr8:48954918-48955179	HepG2	liver:	n/a	chr8:48955089-48955103 chr8:48955031-48955041 chr8:48955093-48955107 chr8:48955094-48955108
29	EP300	chr8:48954803-48955294	HepG2	liver:	n/a	chr8:48955089-48955103 chr8:48955031-48955041 chr8:48955093-48955107 chr8:48955094-48955108
30	FOXA1	chr8:48954887-48955337	HepG2	liver:	n/a	n/a
31	FOXA1	chr8:48954768-48955335	HepG2	liver:	n/a	n/a
32	FOXA1	chr8:48954084-48954496	HepG2	liver:	n/a	n/a
33	FOXA1	chr8:48954728-48955292	HepG2	liver:	n/a	n/a
34	FOXA1	chr8:48954090-48954556	HepG2	liver:	n/a	n/a
35	FOXA1	chr8:48954825-48955269	HepG2	liver:	n/a	n/a
36	FOXA2	chr8:48954459-48955450	HepG2	liver:	n/a	n/a
37	FOXA2	chr8:48954867-48955230	HepG2	liver:	n/a	n/a
38	GATA3	chr8:48931157-48931494	MCF-7	breast:	n/a	n/a
39	HDAC2	chr8:48954872-48955231	HepG2	liver:	n/a	chr8:48955092-48955106 chr8:48955095-48955109 chr8:48955093-48955107 chr8:48955031-48955040 chr8:48955089-48955103 chr8:48955090-48955104 chr8:48955094-48955108
40	HDAC2	chr8:48954784-48955259	HepG2	liver:	n/a	chr8:48955092-48955106 chr8:48955095-48955109 chr8:48955093-48955107 chr8:48955031-48955040 chr8:48955089-48955103 chr8:48955090-48955104 chr8:48955094-48955108
41	HEY1	chr8:48954825-48955110	HepG2	liver:	n/a	n/a
42	HNF4A	chr8:48954862-48955168	HepG2	liver:	n/a	chr8:48954989-48955004
43	HNF4A	chr8:48954791-48955141	HepG2	liver:	n/a	chr8:48954989-48955004
44	HNF4G	chr8:48954890-48955133	HepG2	liver:	n/a	chr8:48954990-48955005
45	IRF1	chr8:48947407-48947457	K562	blood:	n/a	n/a
46	MAFF	chr8:48926219-48926453	HepG2	liver:	n/a	n/a
47	MAFF	chr8:48926213-48926389	K562	blood:	n/a	n/a
48	MAFK	chr8:48926196-48926457	HepG2	liver:	n/a	n/a
49	MAFK	chr8:48926157-48926484	HepG2	liver:	n/a	n/a
50	MAX	chr8:48954842-48955273	HepG2	liver:	n/a	chr8:48955058-48955074

No.	Distal block	Cell Line	Cell type
1	chr8:48920254..48923221-chr8:48935046..48937376,4	MCF-7	breast:
2	chr8:48924792..48926393-chr8:48927338..48929721,2	K562	blood:
3	chr8:48869692..48871263-chr8:48950585..48953419,2	MCF-7	breast:
4	chr8:48933639..48936147-chr8:48936317..48938492,2	K562	blood:
5	chr8:48920860..48923835-chr8:48924077..48926728,4	MCF-7	breast:
6	chr8:48938195..48942344-chr8:48943305..48947689,4	K562	blood:
7	chr8:48943545..48946467-chr8:48947944..48950254,3	K562	blood:
8	chr8:48949897..48951407-chr8:48952676..48954247,2	MCF-7	breast:
9	chr8:48872215..48874076-chr8:48929910..48932503,2	MCF-7	breast:
10	chr8:48949897..48951407-chr8:48952676..48954247,2	MCF-7	breast:
11	chr8:48923260..48926236-chr8:48933537..48935762,2	K562	blood:
12	chr8:48933639..48936147-chr8:48936317..48938492,2	K562	blood:
13	chr8:48920273..48922955-chr8:48929945..48932425,2	MCF-7	breast:
14	chr8:48924342..48926810-chr8:48928221..48931397,3	K562	blood:
15	chr8:48872949..48874764-chr8:48927442..48928965,2	K562	blood:
16	chr8:48943545..48946467-chr8:48947944..48950254,3	K562	blood:
17	chr8:48924792..48926393-chr8:48927338..48929721,2	K562	blood:
18	chr8:48957180..48959047-chr8:48960507..48962710,2	K562	blood:
19	chr8:48938195..48942344-chr8:48943305..48947689,4	K562	blood:
20	chr8:48923287..48925205-chr8:48959755..48962369,2	K562	blood:
21	chr8:48919638..48923031-chr8:48924229..48928095,7	MCF-7	breast:
22	chr8:48881714..48884143-chr8:48924954..48927887,2	MCF-7	breast:
23	chr8:48924342..48926810-chr8:48928221..48931397,3	K562	blood:
24	chr8:48923260..48926236-chr8:48933537..48935762,2	K562	blood:

Variant related genes	Relation type
UBE2V2	TF binding region
ENSG00000169139	chromatin interactions
ENSG00000253729	chromatin interactions
ENSG00000104738	chromatin interactions

Extended variants
information (count: 1103 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:1103 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs571346414	chr8:48924890-48924891	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs114774204	chr8:48925000-48925001	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs139637965	chr8:48925034-48925035	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs187546897	chr8:48925044-48925045	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs144328822	chr8:48925054-48925055	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs554842430	chr8:48925069-48925070	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs573574767	chr8:48925078-48925079	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs567963414	chr8:48925086-48925087	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs573158064	chr8:48925095-48925096	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs530466561	chr8:48925098-48925099	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs192021299	chr8:48925142-48925143	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs373503061	chr8:48925201-48925202	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs559202391	chr8:48925202-48925203	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs577343574	chr8:48925234-48925235	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs138582107	chr8:48925281-48925282	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs545121568	chr8:48925287-48925288	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs531673929	chr8:48925290-48925291	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs563201870	chr8:48925310-48925311	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs530548900	chr8:48925326-48925327	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs542598173	chr8:48925327-48925328	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs561176975	chr8:48925390-48925391	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs528436919	chr8:48925467-48925468	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs546913801	chr8:48925493-48925494	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs181146198	chr8:48925530-48925531	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs146119355	chr8:48925531-48925532	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs532194697	chr8:48925533-48925534	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs368729702	chr8:48925607-48925608	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs372373302	chr8:48925648-48925649	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs569227530	chr8:48925651-48925652	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs536252765	chr8:48925676-48925677	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs561805644	chr8:48925706-48925707	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs566523591	chr8:48925707-48925708	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs184866965	chr8:48925813-48925814	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs573895215	chr8:48925856-48925857	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs534247114	chr8:48925863-48925864	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs563359724	chr8:48925864-48925865	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs539204416	chr8:48925870-48925871	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs75316263	chr8:48925884-48925885	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs35999178	chr8:48925885-48925886	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs558808450	chr8:48925928-48925929	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs376400028	chr8:48925960-48925961	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs112270919	chr8:48925992-48925993	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs542214545	chr8:48926017-48926018	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs557022646	chr8:48926029-48926030	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs75706327	chr8:48926035-48926036	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs575209747	chr8:48926079-48926080	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs542735340	chr8:48926080-48926081	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs560913854	chr8:48926115-48926116	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs572856430	chr8:48926116-48926117	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs149838768	chr8:48926118-48926119	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:96)

Disease	PMID	Source
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
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
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Lung cancer	18438408	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
abnormal development	18461090	CNVD
Cancer	20164920	CNVD
low-grade B-cell lymphoma tumor	18367492	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	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	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
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
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	22286061	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Melanoma	17363583	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
22q11 deletion syndrome	20357662	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Pancreatic cancer	17952125	CNVD
Gastric cancer	22014070	CNVD
Breast cancer	22522925	CNVD
Renal cell carcinoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:743 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:48921600-48931600	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr8:48921600-48931800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr8:48921600-48932400	Weak transcription	Spleen	Spleen
4	chr8:48921600-48932800	Weak transcription	Left Ventricle	heart
5	chr8:48921600-48934200	Weak transcription	Lung	lung
6	chr8:48921600-48956000	Weak transcription	Esophagus	oesophagus
7	chr8:48921600-48957400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr8:48921800-48931200	Weak transcription	Ovary	ovary
9	chr8:48921800-48931800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
10	chr8:48921800-48936200	Weak transcription	Colon Smooth Muscle	Colon
11	chr8:48921800-48943600	Weak transcription	Aorta	Aorta
12	chr8:48921800-48957400	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr8:48921800-48957400	Weak transcription	Placenta Amnion	Placenta Amnion
14	chr8:48921800-48957400	Weak transcription	Stomach Mucosa	stomach
15	chr8:48921800-48960600	Weak transcription	Brain Inferior Temporal Lobe	brain
16	chr8:48921800-48966800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr8:48922000-48931800	Weak transcription	H1 Cell Line	embryonic stem cell
18	chr8:48922000-48931800	Weak transcription	Right Ventricle	heart
19	chr8:48922000-48931800	Weak transcription	Thymus	Thymus
20	chr8:48922000-48932600	Weak transcription	Rectal Mucosa Donor 31	rectum
21	chr8:48922000-48957600	Weak transcription	Colonic Mucosa	Colon
22	chr8:48922200-48931400	Weak transcription	Placenta	Placenta
23	chr8:48922200-48931800	Weak transcription	Fetal Muscle Trunk	muscle
24	chr8:48922200-48932600	Weak transcription	Fetal Intestine Large	intestine
25	chr8:48922200-48932600	Weak transcription	Gastric	stomach
26	chr8:48922200-48932800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
27	chr8:48922200-48934000	Weak transcription	Primary neutrophils fromperipheralblood	blood
28	chr8:48922200-48934200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
29	chr8:48922200-48934800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr8:48922200-48945000	Weak transcription	Psoas Muscle	Psoas
31	chr8:48922200-48947400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr8:48922400-48926400	Weak transcription	HUES6 Cell Line	embryonic stem cell
33	chr8:48922400-48926400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
34	chr8:48922400-48927200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr8:48922400-48930600	Weak transcription	Fetal Kidney	kidney
36	chr8:48922400-48930800	Weak transcription	HUES64 Cell Line	embryonic stem cell
37	chr8:48922400-48930800	Weak transcription	Fetal Heart	heart
38	chr8:48922400-48931000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr8:48922400-48931800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr8:48922400-48931800	Weak transcription	Fetal Lung	lung
41	chr8:48922400-48932400	Weak transcription	Stomach Smooth Muscle	stomach
42	chr8:48922400-48932600	Weak transcription	Brain Angular Gyrus	brain
43	chr8:48922400-48932600	Weak transcription	Monocytes-CD14+_RO01746	blood
44	chr8:48922400-48932800	Weak transcription	Duodenum Smooth Muscle	Duodenum
45	chr8:48922400-48932800	Weak transcription	Rectal Mucosa Donor 29	rectum
46	chr8:48922400-48934200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
47	chr8:48922400-48934400	Weak transcription	Skeletal Muscle Male	skeletal muscle
48	chr8:48922400-48934800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
49	chr8:48922400-48934800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
50	chr8:48922400-48942200	Weak transcription	Brain Hippocampus Middle	brain

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