Variant report

Variant	rs73596325
Chromosome Location	chr10:27203705-27203706
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs11015368	0.94[ASN][1000 genomes]
rs11015369	0.94[ASN][1000 genomes]
rs11015371	0.96[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs11015372	0.94[AFR][1000 genomes];0.91[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs11015373	0.96[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs11527773	0.82[AMR][1000 genomes]
rs12146208	0.92[AFR][1000 genomes]
rs12241317	0.87[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs12241397	0.87[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs12242126	0.94[ASN][1000 genomes]
rs12244030	0.98[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs12244081	0.97[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs12249503	0.93[AFR][1000 genomes]
rs12251191	0.97[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs12252797	0.87[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs12253440	0.95[ASN][1000 genomes]
rs12258372	0.90[AFR][1000 genomes];0.87[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs12260059	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12269045	0.87[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs12411978	0.90[ASN][1000 genomes]
rs12412194	0.97[ASN][1000 genomes]
rs12412850	0.87[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs16927370	0.92[ASN][1000 genomes]
rs16927372	0.92[ASN][1000 genomes]
rs2148115	0.91[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs2182297	0.94[AFR][1000 genomes];0.87[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs2182298	0.92[AFR][1000 genomes]
rs56836829	0.97[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs7074370	0.87[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs7080102	0.82[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs7083364	0.94[AFR][1000 genomes];0.87[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs7089224	0.92[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs7095814	0.92[ASN][1000 genomes]
rs7095977	0.94[AFR][1000 genomes];0.87[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs73596314	0.92[ASN][1000 genomes]
rs73596315	0.92[ASN][1000 genomes]
rs73596317	0.82[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs7894384	0.87[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs7896796	0.87[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs7897673	0.89[ASN][1000 genomes]
rs7897834	0.94[ASN][1000 genomes]
rs7914805	0.82[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs9663679	0.82[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3415799	chr10:26929831-27233591	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	nsv831812	chr10:27061506-27234267	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
3	esv2757376	chr10:27160932-27229993	Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	esv2759740	chr10:27160932-27229993	Strong transcription Bivalent Enhancer Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv430140	chr10:27165095-27227681	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	esv2752390	chr10:27165095-27241780	Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv894978	chr10:27185286-27239820	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	nsv947783	chr10:27192486-27205875	Weak transcription Active TSS Enhancers ZNF genes & repeats Flanking 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	chr10:27203600-27203800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung

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