Variant report

Variant	rs711025
Chromosome Location	chr8:85394387-85394388
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs1039520	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10453097	0.97[ASN][1000 genomes]
rs10504803	0.94[ASN][1000 genomes]
rs10504805	0.80[ASN][1000 genomes]
rs12114244	1.00[ASN][1000 genomes]
rs1319379	1.00[ASN][1000 genomes]
rs13248532	0.97[ASN][1000 genomes]
rs13256410	0.98[ASN][1000 genomes]
rs13257448	0.98[ASN][1000 genomes]
rs13259587	0.97[ASN][1000 genomes]
rs13261209	0.97[ASN][1000 genomes]
rs13265396	0.89[ASN][1000 genomes]
rs13271249	0.97[ASN][1000 genomes]
rs13275430	0.95[ASN][1000 genomes]
rs1351223	0.89[ASN][1000 genomes]
rs1479092	0.88[ASN][1000 genomes]
rs1479093	0.89[ASN][1000 genomes]
rs1479098	0.95[ASN][1000 genomes]
rs1503602	0.95[ASN][1000 genomes]
rs1566791	0.97[ASN][1000 genomes]
rs1824887	0.83[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs1994149	0.81[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs2046313	0.83[ASN][1000 genomes]
rs2127218	0.98[ASN][1000 genomes]
rs28751114	0.97[ASN][1000 genomes]
rs4739691	1.00[ASN][1000 genomes]
rs4740014	1.00[ASN][1000 genomes]
rs4740015	0.84[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs4740016	1.00[ASN][1000 genomes]
rs4740017	1.00[ASN][1000 genomes]
rs4740020	0.97[ASN][1000 genomes]
rs4740021	0.82[ASN][1000 genomes]
rs4740022	0.96[ASN][1000 genomes]
rs4740023	0.92[ASN][1000 genomes]
rs4740024	0.92[ASN][1000 genomes]
rs60533047	0.92[ASN][1000 genomes]
rs6473552	0.86[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs6473553	1.00[ASN][1000 genomes]
rs711007	0.86[AFR][1000 genomes];0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs711011	0.84[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs711027	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs711052	0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs711054	0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs711059	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs711060	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7820792	0.82[ASN][1000 genomes]
rs7829180	0.90[ASN][1000 genomes]
rs7845599	0.82[AFR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831375	chr8:85272352-85463621	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
2	esv3481417	chr8:85279453-86145229	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
3	esv3481418	chr8:85279453-86145229	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 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	chr8:85393800-85394600	Weak transcription	Fetal Intestine Small	intestine
2	chr8:85394000-85394600	Weak transcription	Liver	Liver

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