Variant report

Variant	rs16873925
Chromosome Location	chr8:106916390-106916391
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10097411	0.87[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs10098367	0.81[EUR][1000 genomes]
rs10108222	0.83[EUR][1000 genomes]
rs10955405	0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10955412	0.82[YRI][hapmap]
rs12542647	0.80[CHB][hapmap];0.85[CHD][hapmap];0.94[JPT][hapmap];0.85[ASN][1000 genomes]
rs12676365	0.80[CHB][hapmap];0.94[JPT][hapmap];0.83[ASN][1000 genomes]
rs1353449	0.85[CHB][hapmap];0.93[CHD][hapmap];0.89[GIH][hapmap];0.94[JPT][hapmap]
rs16873932	0.85[ASN][1000 genomes]
rs1813399	0.82[EUR][1000 genomes]
rs6982143	0.82[AFR][1000 genomes]
rs7002447	0.90[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs7013082	0.85[CHB][hapmap];0.93[CHD][hapmap];0.89[GIH][hapmap];0.94[JPT][hapmap]
rs73310947	0.82[AFR][1000 genomes]
rs7814776	0.87[CEU][hapmap];0.85[CHB][hapmap];0.94[JPT][hapmap];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs924101	0.81[AFR][1000 genomes]
rs9283942	0.90[AFR][1000 genomes];0.88[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1021369	chr8:106493317-107243322	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
2	nsv891261	chr8:106880649-106932634	Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv611840	chr8:106913294-107265915	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:106913600-106917400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr8:106915200-106920600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr8:106915200-106930200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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Input of quick search could be:

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

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