Variant report

Variant	rs2348407
Chromosome Location	chr5:94707502-94707503
allele	G/T
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:15)

rs_ID	r²[population]
rs10061291	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1363428	0.88[ASN][1000 genomes]
rs1820041	0.81[EUR][1000 genomes]
rs1895248	0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs1895249	0.82[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs2194089	0.86[ASN][1000 genomes]
rs2432174	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2434251	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs253712	0.85[ASN][1000 genomes]
rs2546097	0.81[EUR][1000 genomes]
rs2546102	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2546103	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2546104	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2560278	0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2731837	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:94706400-94708200	Weak transcription	Fetal Thymus	thymus
2	chr5:94706400-94709400	Weak transcription	Thymus	Thymus

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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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