Variant report

Variant	rs57273810
Chromosome Location	chr15:54816612-54816613
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 75 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:73)

rs_ID	r²[population]
rs16974787	0.83[EUR][1000 genomes]
rs16974800	0.83[EUR][1000 genomes]
rs17237683	0.83[EUR][1000 genomes]
rs17818572	0.83[EUR][1000 genomes]
rs1818706	0.83[EUR][1000 genomes]
rs57439022	0.96[AFR][1000 genomes]
rs58025043	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs58513964	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58750441	0.90[EUR][1000 genomes]
rs58756936	0.98[AFR][1000 genomes]
rs59729248	0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs60711672	0.98[AFR][1000 genomes]
rs60912017	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62022200	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs62022201	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs62022202	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs62022204	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs62022205	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs62022206	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs62022207	0.83[EUR][1000 genomes]
rs62022209	0.83[EUR][1000 genomes]
rs62022210	0.83[EUR][1000 genomes]
rs62022212	0.83[EUR][1000 genomes]
rs62022213	0.83[EUR][1000 genomes]
rs62022398	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs62022400	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62022401	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62022402	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62022403	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs62022404	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62022405	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62022406	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62022409	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs62022410	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62022411	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62022412	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs62022413	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs62022414	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs62022416	0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs62022417	0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs62022419	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs62022420	0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs62022423	0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs62022424	0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs62022425	0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs62022427	0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs62022749	0.83[EUR][1000 genomes]
rs62022751	0.83[EUR][1000 genomes]
rs62022752	0.83[EUR][1000 genomes]
rs62022753	0.83[EUR][1000 genomes]
rs62022758	0.83[EUR][1000 genomes]
rs62022759	0.85[EUR][1000 genomes]
rs62023984	0.83[EUR][1000 genomes]
rs62023985	0.83[EUR][1000 genomes]
rs62023986	0.83[EUR][1000 genomes]
rs62023987	0.83[EUR][1000 genomes]
rs62023988	0.83[EUR][1000 genomes]
rs62023989	0.83[EUR][1000 genomes]
rs62023990	0.83[EUR][1000 genomes]
rs62023992	0.83[EUR][1000 genomes]
rs62023993	0.83[EUR][1000 genomes]
rs7168929	0.81[AMR][1000 genomes]
rs73421550	0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs73421556	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs73421557	0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs74016644	0.94[AFR][1000 genomes]
rs74016645	0.98[AFR][1000 genomes]
rs8024541	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8030914	0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs8040295	0.83[EUR][1000 genomes]
rs8040699	0.83[EUR][1000 genomes]
rs8040891	0.83[EUR][1000 genomes]
rs8041462	0.83[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv817539	chr15:54132584-55095235	Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	nsv1038660	chr15:54756184-55039913	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:54807000-54820600	Weak transcription	Fetal Brain Male	brain
2	chr15:54811000-54869600	Weak transcription	Aorta	Aorta
3	chr15:54816600-54818400	Enhancers	Fetal Lung	lung

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