Variant report

Variant	rs72933056
Chromosome Location	chr2:213535444-213535445
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs10185470	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10195898	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13418296	1.00[ASN][1000 genomes]
rs13418742	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13424239	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16849091	1.00[ASN][1000 genomes]
rs28852185	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6754237	0.82[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs72933024	0.80[EUR][1000 genomes]
rs72933076	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7591655	0.85[AFR][1000 genomes];0.89[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7596833	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	chr2:213531200-213547800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr2:213534200-213535600	Enhancers	H9 Derived Neuron 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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