Variant report

Variant	rs60013975
Chromosome Location	chr1:93853190-93853191
allele	A/T
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:36)

rs_ID	r²[population]
rs11164922	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11811006	0.80[EUR][1000 genomes]
rs12069440	0.97[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs12096122	0.97[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs12404947	0.81[EUR][1000 genomes]
rs12411095	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1582773	0.80[EUR][1000 genomes]
rs17131709	0.81[EUR][1000 genomes]
rs17131710	0.81[EUR][1000 genomes]
rs17131718	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17131741	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1895903	0.80[EUR][1000 genomes]
rs2038698	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs3088371	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs41292137	0.81[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs57710451	0.80[EUR][1000 genomes]
rs60458375	0.81[EUR][1000 genomes]
rs61101021	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs66501175	0.81[EUR][1000 genomes]
rs66804824	0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67002303	0.81[EUR][1000 genomes]
rs67337461	0.81[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs67395827	0.81[EUR][1000 genomes]
rs67723709	0.81[EUR][1000 genomes]
rs67768103	0.81[EUR][1000 genomes]
rs67998457	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs72717334	0.81[EUR][1000 genomes]
rs72717346	0.80[EUR][1000 genomes]
rs72717352	0.81[EUR][1000 genomes]
rs72719120	0.81[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs72719185	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs72959223	0.81[EUR][1000 genomes]
rs72959288	0.81[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs72959296	0.81[AFR][1000 genomes]
rs7339890	0.80[EUR][1000 genomes]
rs900310	0.80[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv871640	chr1:93807122-93953469	Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:93852000-93853200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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