Variant report

Variant	rs7013831
Chromosome Location	chr8:129975177-129975178
allele	C/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]
rs11994519	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16903937	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17241908	1.00[ASN][1000 genomes]
rs17242435	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17820673	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2028518	1.00[ASN][1000 genomes]
rs55865336	1.00[ASN][1000 genomes]
rs56330003	1.00[ASN][1000 genomes]
rs57245121	0.85[EUR][1000 genomes]
rs57247106	0.85[EUR][1000 genomes]
rs57256157	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60136246	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60730791	0.93[EUR][1000 genomes]
rs72728736	1.00[ASN][1000 genomes]
rs9693430	0.93[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:129970800-129982400	Weak transcription	HSMM	muscle
2	chr8:129973000-129976600	Weak transcription	Dnd41	blood

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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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