Variant report

Variant	rs704847
Chromosome Location	chr1:172728931-172728932
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs1102704	0.80[AMR][1000 genomes]
rs2077690	0.88[CHB][hapmap]
rs2131375	0.88[CHB][hapmap]
rs704841	0.88[CHB][hapmap]
rs859622	0.88[CEU][hapmap];0.82[MEX][hapmap];0.85[TSI][hapmap];0.85[EUR][1000 genomes]
rs859629	1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs859631	0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs859633	0.88[CHB][hapmap];0.83[GIH][hapmap];0.85[JPT][hapmap]
rs859641	0.83[AMR][1000 genomes]
rs859723	0.88[CHB][hapmap]
rs859724	0.88[CHB][hapmap]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:172716400-172729400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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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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