Variant report

Variant	rs6451234
Chromosome Location	chr5:35896984-35896985
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs10043573	0.83[EUR][1000 genomes]
rs10053847	0.85[CEU][hapmap];0.81[MEX][hapmap];0.82[TSI][hapmap]
rs10054418	0.90[EUR][1000 genomes]
rs10056484	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10059688	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10070378	0.87[EUR][1000 genomes]
rs10472264	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10472989	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10472990	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11567754	0.85[CEU][hapmap]
rs11567761	0.85[CEU][hapmap]
rs12153578	0.93[JPT][hapmap]
rs13154973	0.87[EUR][1000 genomes]
rs13162685	0.93[EUR][1000 genomes]
rs13167136	0.85[CEU][hapmap]
rs13169780	0.87[EUR][1000 genomes]
rs13169814	0.87[EUR][1000 genomes]
rs13170810	0.95[EUR][1000 genomes]
rs13172065	0.83[EUR][1000 genomes]
rs1389834	0.85[CEU][hapmap];0.81[MEX][hapmap];0.82[TSI][hapmap];0.81[AMR][1000 genomes]
rs1389835	0.84[CEU][hapmap]
rs1494572	0.87[JPT][hapmap]
rs16899999	0.83[EUR][1000 genomes]
rs3822731	0.85[CEU][hapmap]
rs4869430	0.91[EUR][1000 genomes]
rs4869492	0.84[CEU][hapmap]
rs6451236	0.92[EUR][1000 genomes]
rs6451239	0.90[EUR][1000 genomes]
rs6859892	0.90[EUR][1000 genomes]
rs6888699	0.83[EUR][1000 genomes]
rs6891095	0.85[CEU][hapmap]
rs716302	0.87[JPT][hapmap]
rs7381123	0.89[EUR][1000 genomes]
rs7445819	0.92[EUR][1000 genomes]
rs7710177	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7727750	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7736291	0.87[JPT][hapmap]
rs903388	0.81[JPT][hapmap]
rs9292618	0.85[CEU][hapmap];0.81[MEX][hapmap];0.85[TSI][hapmap]
rs991570	0.87[JPT][hapmap]

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	nsv1022761	chr5:35775802-35902546	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv471011	chr5:35861068-36003217	Weak transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS Active TSS Genic enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv830261	chr5:35863084-36018048	Weak transcription ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:35891400-35902400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr5:35893600-35899400	Enhancers	Dnd41	blood
3	chr5:35895200-35898600	Enhancers	Fetal Thymus	thymus
4	chr5:35896400-35897600	Enhancers	Thymus	Thymus

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