Variant report

Variant	rs72631844
Chromosome Location	chr10:28117887-28117888
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:28096701..28099351-chr10:28115513..28118158,2	K562	blood:

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10430558	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10430568	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10826349	0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11006703	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11006704	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11006705	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11006707	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11006708	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11006714	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11006715	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11006717	1.00[EUR][1000 genomes]
rs11006719	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11006720	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11006723	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11006725	1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11006728	1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11006733	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2065689	0.88[ASN][1000 genomes]
rs3737184	1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7077784	0.87[ASN][1000 genomes]
rs72631840	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs72631841	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs72631842	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs72631843	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs72631845	1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72631846	0.84[AMR][1000 genomes]
rs7899995	1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs952404	1.00[EUR][1000 genomes];0.91[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	nsv831813	chr10:28017606-28200651	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv917149	chr10:28018919-28688694	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
3	nsv971859	chr10:28070066-28271252	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 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	chr10:28105600-28127600	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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