Variant report

Variant	rs703608
Chromosome Location	chr12:104009685-104009686
allele	C/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs17494141	1.00[ASN][1000 genomes]
rs17494169	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs17500749	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs17578793	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs4303317	1.00[ASN][1000 genomes]
rs4385985	1.00[ASN][1000 genomes]
rs4612909	1.00[ASN][1000 genomes]
rs697196	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs697197	1.00[CHB][hapmap]
rs697198	1.00[CHB][hapmap]
rs703596	1.00[CHB][hapmap]
rs703597	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs703605	1.00[ASN][1000 genomes]
rs703611	1.00[CHB][hapmap]
rs7133148	1.00[CHB][hapmap]
rs831428	1.00[CHB][hapmap]
rs831429	1.00[CHB][hapmap]
rs831683	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs831686	1.00[ASN][1000 genomes]
rs854249	1.00[CHB][hapmap];1.00[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	nsv1052275	chr12:104008918-104044241	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

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

No data

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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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