Variant report

Variant	rs1414914
Chromosome Location	chr10:97740462-97740463
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10509697	1.00[CHB][hapmap];0.91[JPT][hapmap];0.91[ASN][1000 genomes]
rs11819621	1.00[CHB][hapmap]
rs11819652	1.00[CHB][hapmap]
rs17111247	0.88[ASN][1000 genomes]
rs17111249	0.89[JPT][hapmap];0.91[ASN][1000 genomes]
rs2901895	1.00[CHB][hapmap];0.80[JPT][hapmap];0.88[ASN][1000 genomes]
rs3176882	1.00[CHB][hapmap]
rs3181121	1.00[CHB][hapmap]
rs35557930	0.85[ASN][1000 genomes]
rs57635810	0.91[ASN][1000 genomes]
rs7090375	0.88[ASN][1000 genomes]
rs7093453	1.00[CHB][hapmap]
rs7100644	1.00[CHB][hapmap]
rs7907476	1.00[CHB][hapmap];0.88[ASN][1000 genomes]
rs7909124	1.00[CHB][hapmap];0.88[ASN][1000 genomes]
rs7912552	1.00[CHB][hapmap];0.88[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2761619	chr10:97719520-97746180	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

Quick Search:

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

what's new

Quick links