Variant report

Variant	rs73180849
Chromosome Location	chr21:27982574-27982575
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs12626569	0.84[AMR][1000 genomes]
rs12626994	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs16978623	0.83[EUR][1000 genomes]
rs2409177	1.00[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs55717619	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs55769509	0.84[AMR][1000 genomes]
rs56111541	0.87[EUR][1000 genomes]
rs62215670	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs62215671	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs62215672	1.00[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs62215675	1.00[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs62215676	1.00[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs62215677	1.00[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs62215679	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs62215680	1.00[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs62215681	1.00[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs62216538	0.84[AMR][1000 genomes]
rs62216541	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs62216544	0.82[EUR][1000 genomes]
rs62216546	0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs62216549	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62216553	0.91[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7277801	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7279325	0.87[EUR][1000 genomes]
rs7280270	1.00[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7280561	1.00[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7280624	1.00[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7283578	0.87[EUR][1000 genomes]
rs7283718	0.87[EUR][1000 genomes]
rs73173932	0.87[EUR][1000 genomes]
rs73173933	0.87[EUR][1000 genomes]
rs73173934	0.87[EUR][1000 genomes]
rs73173936	0.87[EUR][1000 genomes]
rs73173938	0.87[EUR][1000 genomes]
rs73173939	0.87[EUR][1000 genomes]
rs870345	1.00[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9980300	0.85[ASN][1000 genomes]

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	nsv1056506	chr21:27332898-28049880	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
2	nsv544412	chr21:27332898-28049880	Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
3	nsv544413	chr21:27942060-28065995	Active TSS Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv913661	chr21:27979924-28025461	Weak transcription Enhancers Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:27981400-27982600	Enhancers	Dnd41	blood

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