Variant report

Variant	rs1956016
Chromosome Location	chr14:63307814-63307815
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs12431729	0.83[CEU][hapmap];0.86[CHB][hapmap]
rs12433909	0.81[CHB][hapmap]
rs171457	0.87[CEU][hapmap];0.86[YRI][hapmap]
rs243146	0.91[CEU][hapmap]
rs243148	1.00[CEU][hapmap];0.93[YRI][hapmap]
rs243149	0.91[CEU][hapmap]
rs243155	0.92[CEU][hapmap];0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs243156	0.91[CEU][hapmap];0.84[EUR][1000 genomes]
rs243157	0.92[CEU][hapmap];0.84[EUR][1000 genomes]
rs243159	0.92[CEU][hapmap]
rs243162	0.91[CEU][hapmap]
rs7155426	0.91[CEU][hapmap]
rs8012941	0.92[CEU][hapmap];0.84[JPT][hapmap]
rs8021413	0.92[CEU][hapmap];0.84[JPT][hapmap]

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	nsv902015	chr14:63261862-63356253	Enhancers Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No data

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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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