Variant report

Variant	rs61500835
Chromosome Location	chr1:79161157-79161158
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 51 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs10493615	0.88[EUR][1000 genomes]
rs1107320	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1109244	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11162523	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11162536	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11162537	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11162539	0.89[EUR][1000 genomes]
rs11162540	0.89[EUR][1000 genomes]
rs11162541	0.89[EUR][1000 genomes]
rs11162544	0.88[EUR][1000 genomes]
rs11587990	0.89[EUR][1000 genomes]
rs12120187	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12128384	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12403117	0.89[EUR][1000 genomes]
rs12409331	0.89[EUR][1000 genomes]
rs12409781	0.89[EUR][1000 genomes]
rs17395034	0.89[EUR][1000 genomes]
rs17395097	0.88[EUR][1000 genomes]
rs17398682	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17399158	0.88[EUR][1000 genomes]
rs17399192	0.88[EUR][1000 genomes]
rs1887286	0.88[EUR][1000 genomes]
rs1926897	0.88[EUR][1000 genomes]
rs1926898	0.88[EUR][1000 genomes]
rs1926901	0.91[EUR][1000 genomes]
rs1926902	0.89[EUR][1000 genomes]
rs1926903	0.89[EUR][1000 genomes]
rs1926904	0.89[EUR][1000 genomes]
rs1926905	0.89[EUR][1000 genomes]
rs273250	0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs58150654	0.89[EUR][1000 genomes]
rs58830966	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs58921479	0.89[EUR][1000 genomes]
rs58945140	0.89[EUR][1000 genomes]
rs58993850	0.89[EUR][1000 genomes]
rs59409549	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs60311076	0.89[EUR][1000 genomes]
rs61613596	0.89[EUR][1000 genomes]
rs61681700	0.89[EUR][1000 genomes]
rs61769988	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs61769992	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61769996	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61770023	0.89[EUR][1000 genomes]
rs61770024	0.89[EUR][1000 genomes]
rs6678067	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7546403	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs975986	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs975987	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[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	nsv871835	chr1:78528803-79501129	Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
2	nsv830315	chr1:79008443-79200591	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
3	nsv491784	chr1:79146141-79853482	Enhancers Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs61500835	IFI44	Cis_1M	lymphoblastoid	RTeQTL

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:79158200-79167200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr1:79158600-79163000	Weak transcription	Osteobl	bone
3	chr1:79160600-79162200	Weak transcription	Muscle Satellite Cultured Cells	--
4	chr1:79160600-79168200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin

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