Variant report

Variant	rs13412593
Chromosome Location	chr2:180538472-180538473
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs10167651	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10168158	0.90[AFR][1000 genomes];0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10178197	0.89[ASN][1000 genomes]
rs10187687	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10190718	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10201348	0.89[ASN][1000 genomes]
rs10497546	0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10497547	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11889892	0.99[ASN][1000 genomes]
rs11897834	0.96[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11903667	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12463735	0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12465360	0.96[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12477618	0.96[ASN][1000 genomes]
rs1399690	0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1515285	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1515293	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1554105	0.96[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1606817	0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs16866924	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs16866929	0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs28469228	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs28615198	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6433801	0.91[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6708429	0.99[ASN][1000 genomes]
rs6708458	0.99[ASN][1000 genomes]
rs6730056	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6760409	0.96[AFR][1000 genomes];0.87[AMR][1000 genomes];0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs72958954	0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs72958970	0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs72958973	0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7557526	0.86[ASN][1000 genomes]
rs7569504	0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7569621	0.96[ASN][1000 genomes]
rs7570893	0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7581866	0.88[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs7607628	0.89[ASN][1000 genomes]

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:180535200-180540200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr2:180536200-180541600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr2:180536800-180539400	Weak transcription	Gastric	stomach
4	chr2:180536800-180541200	Weak transcription	HSMMtube	muscle
5	chr2:180537400-180542400	Weak transcription	Fetal Intestine Large	intestine

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