Variant report

Variant	rs56397364
Chromosome Location	chr14:63239078-63239079
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]
rs1021346	1.00[AFR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11158452	0.87[ASN][1000 genomes]
rs12433281	0.95[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs12882526	0.84[AFR][1000 genomes]
rs12891322	0.91[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs12891982	0.95[AFR][1000 genomes]
rs12893269	0.81[AFR][1000 genomes]
rs2171876	0.93[AMR][1000 genomes];0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs35679534	0.95[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs35872261	0.84[AFR][1000 genomes]
rs7493979	0.91[ASN][1000 genomes]
rs961066	1.00[AFR][1000 genomes];0.89[AMR][1000 genomes]

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:63227200-63246400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr14:63233200-63248800	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr14:63237400-63243200	Weak transcription	Skeletal Muscle Female	skeletal muscle

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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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