Variant report

Variant	rs17288495
Chromosome Location	chr6:45764140-45764141
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 70 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:67)

rs_ID	r²[population]
rs10498763	0.92[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs167680	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16873787	0.92[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs16873788	0.92[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs16873790	0.92[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs16873791	0.92[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs16873793	0.89[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs16873804	0.92[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs16873805	0.92[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs16873808	0.92[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs16873809	0.92[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs16873810	0.92[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs16873811	0.92[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs16873820	0.92[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs16873823	0.92[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs16873825	0.92[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs16873831	0.92[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs16873834	0.92[AMR][1000 genomes]
rs16873841	0.92[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs16873850	0.89[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17209944	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17209951	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17216353	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17216367	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17216374	1.00[AFR][1000 genomes]
rs17216395	1.00[AFR][1000 genomes]
rs17288467	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17288481	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2122286	1.00[AFR][1000 genomes]
rs321328	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs57475247	0.92[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs57565233	0.92[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs60012321	0.92[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs61102292	0.92[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs62400427	0.94[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs62400429	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62400435	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62400439	0.92[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs62400440	0.89[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs62400441	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62400453	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62400454	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62400455	0.92[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs62400456	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62400457	0.92[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs62401860	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62401861	0.97[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs62401862	0.94[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs62401863	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62401864	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62401866	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62401867	1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62401868	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62401869	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62401871	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62401877	1.00[AFR][1000 genomes]
rs62401881	1.00[AFR][1000 genomes]
rs62401883	1.00[AFR][1000 genomes]
rs6458463	0.92[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6458465	0.92[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6458466	0.92[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7744982	0.92[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7747594	0.92[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7752476	0.92[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7752583	0.92[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7767214	0.92[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7773377	0.92[AMR][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	nsv1028393	chr6:44875558-45822335	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
2	nsv538211	chr6:44875558-45822335	ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
3	nsv532024	chr6:45475088-45982640	Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 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	chr6:45763600-45764800	Weak transcription	Fetal Muscle Leg	muscle
2	chr6:45763600-45780600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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