Variant report

Variant	rs7155426
Chromosome Location	chr14:63305700-63305701
allele	C/G
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]
rs11846438	0.87[CEU][hapmap];0.81[JPT][hapmap]
rs12431729	0.95[CEU][hapmap];0.88[EUR][1000 genomes]
rs12883703	0.87[CEU][hapmap]
rs171457	0.82[CEU][hapmap];0.84[CHB][hapmap]
rs1956016	0.91[CEU][hapmap]
rs1980561	0.87[CEU][hapmap];0.85[CHB][hapmap]
rs243146	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs243148	0.92[CEU][hapmap];0.95[CHB][hapmap]
rs243149	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap]
rs243155	1.00[CEU][hapmap];0.90[JPT][hapmap];0.87[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs243156	1.00[CEU][hapmap];0.84[JPT][hapmap];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs243157	1.00[CEU][hapmap];0.86[JPT][hapmap];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs243159	1.00[CEU][hapmap]
rs243162	1.00[CEU][hapmap]
rs8012941	0.83[CEU][hapmap]
rs8021413	0.83[CEU][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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