Variant report

Variant	rs4468444
Chromosome Location	chr12:105987568-105987569
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:35)

rs_ID	r²[population]
rs10735407	0.81[ASN][1000 genomes]
rs10861456	0.81[EUR][1000 genomes]
rs10861457	0.81[EUR][1000 genomes]
rs10861461	0.82[ASN][1000 genomes]
rs11112595	0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11112596	0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1317555	0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1526844	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1526846	0.85[ASN][1000 genomes]
rs1806811	0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1997174	0.81[EUR][1000 genomes]
rs2049571	0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2049572	0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2374514	0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2374515	0.83[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2694388	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2694390	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2694394	0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2694395	0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2694398	0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2694399	0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2694400	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2694401	0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2694404	0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2711732	0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2711734	0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2711735	0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2711736	0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2711737	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2711739	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2711741	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2888859	0.94[AMR][1000 genomes];0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs876929	0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs885131	0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs941105	0.89[EUR][1000 genomes];0.90[ASN][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	nsv832507	chr12:105821685-106005186	Enhancers ZNF genes & repeats Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv1039068	chr12:105935786-106211250	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:105982200-105989200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr12:105982200-105989400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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