Variant report

Variant	rs158968
Chromosome Location	chr5:57941969-57941970
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs1019469	0.86[JPT][hapmap]
rs1035394	0.82[JPT][hapmap]
rs158965	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs158969	0.86[AFR][1000 genomes];0.94[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs158970	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[YRI][hapmap];0.86[AFR][1000 genomes];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs158974	0.82[YRI][hapmap];0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs158979	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs17346755	0.85[CEU][hapmap];0.84[JPT][hapmap];0.83[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs2591914	0.95[JPT][hapmap];0.83[YRI][hapmap];0.87[ASN][1000 genomes]
rs292970	1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs292971	0.83[YRI][hapmap];0.86[AMR][1000 genomes]
rs292982	0.82[YRI][hapmap];0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs292985	0.82[YRI][hapmap];0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs292992	0.84[AFR][1000 genomes];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs389543	0.86[AMR][1000 genomes]
rs393400	0.85[AMR][1000 genomes]
rs433188	0.83[YRI][hapmap];0.86[AMR][1000 genomes]
rs434759	0.86[AMR][1000 genomes]
rs435514	0.85[CEU][hapmap];0.91[YRI][hapmap];0.85[AFR][1000 genomes];0.86[AMR][1000 genomes]
rs442414	0.83[YRI][hapmap];0.86[AMR][1000 genomes]
rs449867	1.00[YRI][hapmap];0.82[AFR][1000 genomes];0.86[AMR][1000 genomes]
rs452321	0.86[AMR][1000 genomes]
rs965795	0.81[JPT][hapmap]
rs984664	0.82[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2830363	chr5:57893949-58555491	Weak transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	nsv1029145	chr5:57905821-58141221	Active TSS Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv830311	chr5:57912546-58105636	Enhancers Active TSS Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv1020937	chr5:57938969-57959918	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region 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	chr5:57933600-57944000	Weak transcription	Pancreatic Islets	Pancreatic Islet

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