Variant report

Variant	rs61897704
Chromosome Location	chr11:119675331-119675332
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs10750166	1.00[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs10892472	0.84[ASN][1000 genomes]
rs10892474	0.84[ASN][1000 genomes]
rs11217524	0.84[ASN][1000 genomes]
rs1447149	0.84[ASN][1000 genomes]
rs61897703	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61897705	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7125270	0.84[ASN][1000 genomes]
rs73577182	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7926586	0.92[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:119666400-119676000	Weak transcription	Right Ventricle	heart
2	chr11:119672400-119678600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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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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