Variant report

Variant	rs10095187
Chromosome Location	chr8:10050738-10050739
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs10104376	1.00[EUR][1000 genomes]
rs10107815	1.00[EUR][1000 genomes]
rs12334619	1.00[EUR][1000 genomes]
rs13362873	1.00[EUR][1000 genomes]
rs17151175	1.00[EUR][1000 genomes]
rs17151195	1.00[EUR][1000 genomes]
rs17151325	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28595664	1.00[EUR][1000 genomes]
rs28674018	1.00[EUR][1000 genomes]
rs60515866	1.00[EUR][1000 genomes]
rs6984706	1.00[EUR][1000 genomes]
rs6999817	1.00[EUR][1000 genomes]
rs73530939	1.00[EUR][1000 genomes]
rs73662805	1.00[EUR][1000 genomes]
rs9329217	1.00[EUR][1000 genomes]
rs9657534	1.00[EUR][1000 genomes]
rs9657537	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv610263	chr8:9941021-10090149	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
2	nsv831230	chr8:9953343-10139350	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
3	nsv1027280	chr8:9958259-10058984	Enhancers Active TSS Genic enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv1021921	chr8:9958259-10212555	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv890344	chr8:9995515-10060638	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	nsv831231	chr8:10001214-10189094	Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	nsv1026335	chr8:10037279-10139782	Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:10048200-10052200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr8:10049000-10051200	Enhancers	Fetal Brain Male	brain
3	chr8:10049400-10050800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr8:10049400-10051000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr8:10049600-10051000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr8:10049800-10050800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr8:10049800-10050800	Enhancers	Muscle Satellite Cultured Cells	--
8	chr8:10050000-10051000	Enhancers	Fetal Brain Female	brain
9	chr8:10050000-10057800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr8:10050000-10068000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr8:10050200-10053600	Weak transcription	Primary neutrophils fromperipheralblood	blood
12	chr8:10050400-10054600	Weak transcription	HMEC	breast
13	chr8:10050400-10054600	Weak transcription	NHEK	skin
14	chr8:10050400-10055000	Weak transcription	HSMMtube	muscle
15	chr8:10050400-10058000	Weak transcription	Aorta	Aorta
16	chr8:10050600-10050800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr8:10050600-10054800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr8:10050600-10055000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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