Variant report

Variant	rs10092306
Chromosome Location	chr8:85154489-85154490
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs10102752	0.83[EUR][1000 genomes]
rs10102848	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10112333	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10112823	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12682650	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs13253565	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13253923	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs13261079	0.89[ASN][1000 genomes]
rs13261650	0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs13265288	0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13266356	0.83[EUR][1000 genomes]
rs13268314	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs13273191	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13281165	0.95[ASN][1000 genomes]
rs13281339	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1352823	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1388412	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1472101	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1491555	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1491556	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1907548	0.95[ASN][1000 genomes]
rs2130985	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs28378543	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2895920	0.82[EUR][1000 genomes]
rs4392892	0.93[ASN][1000 genomes]
rs4509323	0.82[EUR][1000 genomes]
rs4518663	0.95[ASN][1000 genomes]
rs4644249	0.92[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4740004	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs6473536	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6996404	0.99[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7825715	0.82[EUR][1000 genomes]
rs7829111	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7829286	0.82[EUR][1000 genomes]
rs7841089	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7846520	0.81[AMR][1000 genomes]
rs977857	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs977858	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs977859	0.81[AMR][1000 genomes];0.82[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	esv2753846	chr8:84637092-85239703	Active TSS Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv831374	chr8:85103604-85308976	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 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	chr8:85150400-85155800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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