Variant report

Variant	rs73260787
Chromosome Location	chr10:44150906-44150907
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10450466	0.87[AFR][1000 genomes]
rs17154095	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17154102	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17154123	0.86[AFR][1000 genomes]
rs41422044	0.94[AFR][1000 genomes]
rs4491169	0.87[AFR][1000 genomes]
rs4614393	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4623849	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57401751	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57895085	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58585102	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73260769	0.91[AFR][1000 genomes]
rs73260775	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73260776	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73260778	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73260785	0.87[AFR][1000 genomes]
rs73260790	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73260791	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73260793	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73260799	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73262703	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73262705	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73262706	0.81[AFR][1000 genomes]
rs73262710	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73264462	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73264498	0.94[AFR][1000 genomes]
rs872533	0.94[AFR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:44145000-44153600	Weak transcription	Fetal Stomach	stomach
2	chr10:44149400-44153200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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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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