Variant report

Variant	nsv516599
Chromosome Location	chr8:67423997-67432106
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:42)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:4)

No data

(count:42 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:67345421..67347646-chr8:67424128..67426947,2	MCF-7	breast:
2	chr8:67424639..67425515-chr8:67626021..67627124,4	MCF-7	breast:
3	chr8:67398115..67399973-chr8:67424030..67426495,2	MCF-7	breast:
4	chr8:67424089..67425027-chr8:67520588..67521105,2	MCF-7	breast:
5	chr8:67429586..67437602-chr8:67518154..67525527,12	MCF-7	breast:
6	chr8:67424749..67427225-chr8:67428836..67431636,2	K562	blood:
7	chr8:67370490..67380541-chr8:67430312..67436911,14	MCF-7	breast:
8	chr8:67426610..67429347-chr8:67484822..67487223,2	MCF-7	breast:
9	chr8:67424489..67425356-chr8:67521366..67522501,3	MCF-7	breast:
10	chr8:67429729..67439141-chr8:67513957..67529788,42	MCF-7	breast:
11	chr8:67430877..67432453-chr8:67473862..67476389,2	MCF-7	breast:
12	chr2:163798580..163801133-chr8:67428520..67431198,2	MCF-7	breast:
13	chr8:67371694..67372212-chr8:67424421..67425018,2	MCF-7	breast:
14	chr8:67424386..67425010-chr8:67524674..67525587,2	MCF-7	breast:
15	chr8:67426758..67428593-chr8:145751587..145753777,2	MCF-7	breast:
16	chr8:67424552..67425654-chr8:67434384..67435380,10	MCF-7	breast:
17	chr8:67424716..67425333-chr8:67434436..67435290,5	MCF-7	breast:
18	chr8:67424694..67427156-chr8:67976156..67978565,3	MCF-7	breast:
19	chr8:67385971..67387776-chr8:67424804..67426337,2	MCF-7	breast:
20	chr8:67424243..67425486-chr8:67521356..67522211,7	MCF-7	breast:
21	chr8:67423253..67428167-chr8:67524174..67527584,6	MCF-7	breast:
22	chr8:67424259..67425739-chr8:67434384..67435598,12	MCF-7	breast:
23	chr8:67342992..67344694-chr8:67430908..67432583,2	MCF-7	breast:
24	chr8:67429832..67432684-chr8:67975260..67977974,2	MCF-7	breast:
25	chr8:67428847..67430919-chr8:67577897..67580130,2	MCF-7	breast:
26	chr8:67423189..67428522-chr8:67623234..67628071,7	MCF-7	breast:
27	chr8:67351396..67355206-chr8:67431500..67436030,5	MCF-7	breast:
28	chr8:67424749..67427225-chr8:67428836..67431636,2	K562	blood:
29	chr8:67431908..67437032-chr8:67623228..67628487,25	MCF-7	breast:
30	chr8:67370581..67378448-chr8:67424626..67427789,7	MCF-7	breast:
31	chr8:67428848..67431240-chr8:67434976..67437529,2	K562	blood:
32	chr8:67425103..67425812-chr8:67434842..67435368,2	MCF-7	breast:
33	chr8:67424863..67425423-chr8:67446937..67447756,2	MCF-7	breast:
34	chr8:67422088..67426308-chr8:67518696..67523583,8	MCF-7	breast:
35	chr8:67424158..67425815-chr8:67434087..67435662,5	MCF-7	breast:
36	chr8:67417099..67419629-chr8:67424131..67426273,2	MCF-7	breast:
37	chr8:67424767..67425416-chr8:67625919..67627124,5	MCF-7	breast:
38	chr8:67424323..67425873-chr8:67625321..67626734,5	MCF-7	breast:
39	chr8:67421561..67429070-chr8:67518939..67527775,32	MCF-7	breast:
40	chr8:67429685..67437301-chr8:67452387..67457412,12	MCF-7	breast:
41	chr8:67340281..67342191-chr8:67431745..67435252,3	MCF-7	breast:
42	chr8:67422601..67431884-chr8:67622296..67628668,31	MCF-7	breast:

No data

(count:4 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	C8orf46	hsa-miR-192-5p	chr8:67429349-67429356
2	C8orf46	hsa-miR-215-5p	chr8:67429349-67429356
3	C8orf46	hsa-miR-192-5p	chr8:67429335-67429356
4	C8orf46	hsa-miR-215-5p	chr8:67429335-67429356

Variant related genes	Relation type
ENSG00000179041	chromatin interactions
ENSG00000213865	chromatin interactions
ENSG00000147576	chromatin interactions
ENSG00000270024	chromatin interactions
ENSG00000104218	chromatin interactions
ENSG00000104205	chromatin interactions
ENSG00000254402	chromatin interactions
ENSG00000121022	chromatin interactions
ENSG00000246145	chromatin interactions
ENSG00000169085	chromatin interactions
ENSG00000185697	chromatin interactions
ENSG00000175073	chromatin interactions

Extended variants
information (count: 354 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:354 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12541034	chr8:67423997-67423998	Enhancers ZNF genes & repeats Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs562955551	chr8:67424053-67424054	Enhancers ZNF genes & repeats Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs2004791	chr8:67424066-67424067	Enhancers ZNF genes & repeats Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs143112739	chr8:67424067-67424068	Enhancers ZNF genes & repeats Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs138730807	chr8:67424089-67424090	Enhancers ZNF genes & repeats Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs533401374	chr8:67424117-67424118	Enhancers ZNF genes & repeats Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs201411384	chr8:67424122-67424123	Enhancers ZNF genes & repeats Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs374242133	chr8:67424157-67424158	Enhancers ZNF genes & repeats Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs142725196	chr8:67424159-67424160	Enhancers ZNF genes & repeats Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs535065679	chr8:67424194-67424195	Enhancers ZNF genes & repeats Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs548694081	chr8:67424201-67424202	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs147364585	chr8:67424245-67424246	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs35689084	chr8:67424301-67424302	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs376693961	chr8:67424319-67424320	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs538057035	chr8:67424357-67424358	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs139443714	chr8:67424439-67424440	Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs577875340	chr8:67424443-67424444	Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs16932940	chr8:67424464-67424465	Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs79554479	chr8:67424470-67424471	Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs557765994	chr8:67424498-67424499	Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs574117741	chr8:67424501-67424502	Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs571154560	chr8:67424513-67424514	Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs187059115	chr8:67424545-67424546	Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs539785270	chr8:67424555-67424556	Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs562992384	chr8:67424561-67424562	Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs576425381	chr8:67424571-67424572	Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs111971952	chr8:67424580-67424581	Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs556450422	chr8:67424581-67424582	Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs16932942	chr8:67424586-67424587	Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs150687479	chr8:67424587-67424588	Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs118137615	chr8:67424624-67424625	Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs561221743	chr8:67424625-67424626	Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs7008554	chr8:67424654-67424655	Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs746789	chr8:67424669-67424670	Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs568939795	chr8:67424670-67424671	Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs34763285	chr8:67424675-67424676	Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs386726311	chr8:67424677-67424678	Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs34386914	chr8:67424678-67424679	Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs571393693	chr8:67424706-67424707	Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs533962224	chr8:67424758-67424759	Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs192659729	chr8:67424772-67424773	Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs567541354	chr8:67424841-67424842	Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs536661685	chr8:67424892-67424893	Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs541162838	chr8:67424931-67424932	Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs62512586	chr8:67424963-67424964	Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs149829319	chr8:67425000-67425001	Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
47	rs736458	chr8:67425037-67425038	Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs543791499	chr8:67425069-67425070	Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
49	rs558992981	chr8:67425089-67425090	Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
50	rs3065712	chr8:67425091-67425092	Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:94)

Disease	PMID	Source
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
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	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
Multiple myeloma	16461302	CNVD
abnormal development	18461090	CNVD
Cancer	20164920	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
Cancer	16751803	CNVD
Salivary gland tumor	18059337	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
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
Melanoma	22183965	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Sezary syndrome	18413736	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Adenoid cystic carcinoma	18332873	CNVD

Chromatin state (count:384 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:67414800-67424400	Weak transcription	Hela-S3	cervix
2	chr8:67416000-67424400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr8:67419800-67424600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr8:67419800-67430000	Weak transcription	Psoas Muscle	Psoas
5	chr8:67420000-67424400	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr8:67420000-67424400	Weak transcription	HUES64 Cell Line	embryonic stem cell
7	chr8:67420000-67424400	Weak transcription	Fetal Kidney	kidney
8	chr8:67420000-67427600	Weak transcription	Liver	Liver
9	chr8:67420400-67424400	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr8:67420400-67424400	Weak transcription	HUVEC	blood vessel
11	chr8:67420400-67424600	Weak transcription	Fetal Lung	lung
12	chr8:67420600-67424200	Weak transcription	Muscle Satellite Cultured Cells	--
13	chr8:67420600-67424400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr8:67420600-67424400	Weak transcription	Ovary	ovary
15	chr8:67420600-67424400	Weak transcription	NH-A	brain
16	chr8:67420600-67424400	Weak transcription	Osteobl	bone
17	chr8:67420600-67424600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
18	chr8:67420600-67424600	Weak transcription	Colon Smooth Muscle	Colon
19	chr8:67420600-67424600	Weak transcription	Right Atrium	heart
20	chr8:67420600-67425400	Weak transcription	Primary T helper cells fromperipheralblood	blood
21	chr8:67420600-67425600	Weak transcription	Primary T helper cells PMA-I stimulated	--
22	chr8:67420800-67424400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr8:67420800-67424400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr8:67420800-67424400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr8:67420800-67424400	Weak transcription	Left Ventricle	heart
26	chr8:67420800-67424400	Weak transcription	Pancreas	Pancrea
27	chr8:67420800-67424400	Weak transcription	Right Ventricle	heart
28	chr8:67420800-67424400	Weak transcription	Spleen	Spleen
29	chr8:67420800-67424400	Weak transcription	NHEK	skin
30	chr8:67420800-67424400	Weak transcription	NHLF	lung
31	chr8:67420800-67424600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr8:67421000-67424200	Weak transcription	HSMMtube	muscle
33	chr8:67421000-67424400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr8:67421000-67424400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr8:67421000-67424400	Weak transcription	A549	lung
36	chr8:67421000-67424400	Weak transcription	NHDF-Ad	bronchial
37	chr8:67421000-67424600	Weak transcription	Placenta Amnion	Placenta Amnion
38	chr8:67421000-67426000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
39	chr8:67421200-67424600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
40	chr8:67421400-67424400	Weak transcription	Rectal Smooth Muscle	rectum
41	chr8:67421600-67424800	Enhancers	Skeletal Muscle Male	skeletal muscle
42	chr8:67422200-67424400	Weak transcription	GM12878-XiMat	blood
43	chr8:67422600-67424600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr8:67422800-67424400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr8:67422800-67425000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr8:67423000-67424000	Genic enhancers	Brain Angular Gyrus	brain
47	chr8:67423000-67424200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr8:67423000-67424200	Weak transcription	HMEC	breast
49	chr8:67423000-67424600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr8:67423200-67424400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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