Variant report

Variant	rs57256097
Chromosome Location	chr5:126816667-126816668
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 50 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs11950427	0.84[EUR][1000 genomes]
rs17444885	0.94[EUR][1000 genomes]
rs17604882	0.92[EUR][1000 genomes]
rs17604889	0.92[EUR][1000 genomes]
rs17604946	0.92[EUR][1000 genomes]
rs17673474	0.92[EUR][1000 genomes]
rs17673517	0.92[EUR][1000 genomes]
rs17673685	0.93[EUR][1000 genomes]
rs17673995	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17763722	0.91[ASN][1000 genomes]
rs17839690	0.81[EUR][1000 genomes]
rs2408871	0.84[EUR][1000 genomes]
rs3812053	0.93[EUR][1000 genomes]
rs41298308	0.93[EUR][1000 genomes]
rs41298312	0.93[EUR][1000 genomes]
rs6874752	0.84[EUR][1000 genomes]
rs6882034	0.95[EUR][1000 genomes]
rs72790405	0.92[EUR][1000 genomes]
rs72790408	0.92[EUR][1000 genomes]
rs72790410	0.92[EUR][1000 genomes]
rs72790411	0.92[EUR][1000 genomes]
rs72790412	0.92[EUR][1000 genomes]
rs72790417	0.88[EUR][1000 genomes]
rs72790418	0.93[EUR][1000 genomes]
rs72790419	0.93[EUR][1000 genomes]
rs72790422	0.84[EUR][1000 genomes]
rs72790424	0.84[EUR][1000 genomes]
rs72790426	0.84[EUR][1000 genomes]
rs72790428	0.93[EUR][1000 genomes]
rs72790430	0.93[EUR][1000 genomes]
rs72790433	0.93[EUR][1000 genomes]
rs72790438	0.93[EUR][1000 genomes]
rs72790444	0.93[EUR][1000 genomes]
rs72790451	0.93[EUR][1000 genomes]
rs72790460	0.95[EUR][1000 genomes]
rs72790468	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72790470	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72790475	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72790483	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72790485	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72790487	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73786108	0.95[EUR][1000 genomes]
rs7718640	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7730171	0.90[AFR][1000 genomes];0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7731380	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1033607	chr5:126385181-127304459	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
2	nsv1019821	chr5:126658200-126934917	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	nsv537894	chr5:126658200-126934917	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
4	nsv1032587	chr5:126691103-126826978	Genic enhancers Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv830478	chr5:126721368-126937408	Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 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	chr5:126789800-126830400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr5:126815800-126817200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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