Variant report

Variant	rs3128244
Chromosome Location	chr10:44120534-44120535
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Variant related genes	Relation type
ZNF32-AS3	TF binding region
ENSG00000237389	Chromatin interaction
ENSG00000169813	Chromatin interaction
ENSG00000238263	Chromatin interaction

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

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

rs_ID	r²[population]
rs3123656	0.91[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs3123658	0.91[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs3123660	0.91[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs3123664	0.91[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs3123665	0.91[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs3123672	0.91[AMR][1000 genomes];0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs3123675	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs3128246	0.96[AMR][1000 genomes];0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs3128248	0.82[ASN][1000 genomes]
rs3128251	0.91[AMR][1000 genomes];0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:44119200-44123800	Weak transcription	Primary T helper memory cells from peripheral blood 2	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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