Variant report

Variant	rs62497458
Chromosome Location	chr7:96719089-96719090
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10269566	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10499934	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11972827	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1343646	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17168169	0.94[EUR][1000 genomes]
rs28458266	0.91[EUR][1000 genomes]
rs2894101	0.94[EUR][1000 genomes]
rs4493838	0.85[ASN][1000 genomes]
rs55844717	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs56130919	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6465569	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs66801005	0.87[EUR][1000 genomes]
rs6946160	0.85[EUR][1000 genomes]
rs73233818	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs73233828	1.00[AFR][1000 genomes]
rs7811543	0.95[EUR][1000 genomes]

No data

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

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

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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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