Variant report

Variant	rs1853131
Chromosome Location	chr6:85922851-85922852
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 65 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:63)

rs_ID	r²[population]
rs10944093	1.00[ASN][1000 genomes]
rs10944094	0.93[EUR][1000 genomes]
rs12206706	1.00[ASN][1000 genomes]
rs12211596	1.00[ASN][1000 genomes]
rs1321733	0.92[EUR][1000 genomes]
rs1321745	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1321747	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1321750	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1321751	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1321752	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1407154	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1407155	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1407168	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1535313	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1547702	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1570108	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1590235	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1590236	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1590237	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1853125	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1853126	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1853129	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1853130	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1885016	0.87[ASN][1000 genomes]
rs1958940	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1981018	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2183944	0.82[EUR][1000 genomes]
rs2210479	0.93[EUR][1000 genomes]
rs4053812	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4363008	1.00[ASN][1000 genomes]
rs4400187	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4484492	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4707141	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4707142	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4707143	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs504604	0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs525779	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs537411	0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs550481	0.93[EUR][1000 genomes]
rs552249	0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs554187	0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs559487	0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs562380	0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6454456	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6922736	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6937238	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6941709	0.87[ASN][1000 genomes]
rs700499	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs700500	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs700502	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs700506	0.88[EUR][1000 genomes]
rs721753	0.87[ASN][1000 genomes]
rs72918312	0.87[ASN][1000 genomes]
rs7753409	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7762165	0.91[EUR][1000 genomes]
rs7771273	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7772310	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9342025	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9344467	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9344468	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9351040	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9353253	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9353292	0.93[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	nsv1017418	chr6:85344786-86259540	Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Enhancers Bivalent/Poised TSS Strong transcription Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
2	nsv538347	chr6:85344786-86259540	Weak transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 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	chr6:85922600-85923000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr6:85922800-85923200	Enhancers	HepG2	liver

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