Variant report

Variant	rs17168169
Chromosome Location	chr7:96720001-96720002
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs10269566	0.86[CEU][hapmap];0.88[EUR][1000 genomes]
rs10499934	0.86[CEU][hapmap];0.88[EUR][1000 genomes]
rs11972827	0.88[EUR][1000 genomes]
rs11976587	0.82[CEU][hapmap]
rs11984368	0.81[CEU][hapmap]
rs12670377	0.81[CEU][hapmap];0.81[CHB][hapmap];0.82[JPT][hapmap]
rs1343646	0.88[EUR][1000 genomes]
rs2037782	0.81[CEU][hapmap]
rs28458266	0.88[EUR][1000 genomes]
rs2894101	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs55844717	0.88[EUR][1000 genomes]
rs56130919	0.88[EUR][1000 genomes]
rs62497458	0.94[EUR][1000 genomes]
rs6465569	0.87[CEU][hapmap];0.88[EUR][1000 genomes]
rs66801005	0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6946160	0.83[EUR][1000 genomes]
rs73233818	0.88[EUR][1000 genomes]
rs7811543	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:96719000-96720400	Enhancers	Fetal Brain Male	brain
2	chr7:96720000-96720600	Enhancers	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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