Variant report

Variant	rs10957026
Chromosome Location	chr8:49216242-49216243
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs1027966	0.87[CHB][hapmap];0.87[JPT][hapmap];0.87[ASN][1000 genomes]
rs10957025	0.81[ASN][1000 genomes]
rs13273513	0.97[ASN][1000 genomes]
rs16936623	0.82[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs34664131	0.81[ASN][1000 genomes]
rs4873082	0.98[ASN][1000 genomes]
rs4873274	0.96[ASN][1000 genomes]
rs7008284	0.80[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831310	chr8:49080177-49256440	Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv831311	chr8:49106160-49290209	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv1018242	chr8:49190915-49243694	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv539600	chr8:49190915-49243694	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:49210800-49216400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr8:49210800-49217200	Weak transcription	NHLF	lung
3	chr8:49215000-49216600	Enhancers	HMEC	breast
4	chr8:49215200-49217800	Enhancers	Muscle Satellite Cultured Cells	--
5	chr8:49215600-49217400	Weak transcription	NHDF-Ad	bronchial
6	chr8:49216000-49216400	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr8:49216000-49217000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr8:49216000-49217400	Weak transcription	Osteobl	bone
9	chr8:49216200-49216600	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr8:49216200-49216600	ZNF genes & repeats	Esophagus	oesophagus

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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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