Variant report

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10230632	0.93[ASN][1000 genomes]
rs10230965	0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10232401	0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10243297	0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10245559	0.93[ASN][1000 genomes]
rs10246093	0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10251475	0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10251597	0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10271590	1.00[ASN][1000 genomes]
rs12381410	0.82[EUR][1000 genomes]
rs12386692	0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1560214	0.85[ASN][1000 genomes]
rs2562730	0.85[ASN][1000 genomes]
rs2562734	0.85[ASN][1000 genomes]
rs2562737	0.82[ASN][1000 genomes]
rs2562740	0.89[ASN][1000 genomes]
rs2732394	0.85[ASN][1000 genomes]
rs2732432	0.86[ASN][1000 genomes]
rs28479078	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28525628	0.80[EUR][1000 genomes]
rs28526579	0.81[EUR][1000 genomes]
rs28670000	0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs28788212	0.86[EUR][1000 genomes]
rs3097361	0.89[ASN][1000 genomes]
rs35586323	0.85[ASN][1000 genomes]
rs3958071	0.93[ASN][1000 genomes]
rs4642561	0.81[EUR][1000 genomes]
rs4728108	0.85[ASN][1000 genomes]
rs4731455	0.82[ASN][1000 genomes]
rs5009156	1.00[ASN][1000 genomes]
rs6467178	0.85[ASN][1000 genomes]
rs6467190	0.83[EUR][1000 genomes]
rs6947697	0.82[ASN][1000 genomes]
rs73463166	0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs73465114	0.82[EUR][1000 genomes]
rs7797240	0.96[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1794896	chr7:128142170-128170380	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs58979384	RP11-274B21.4	cis	Whole Blood	GTEx

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:128117800-128162800	Weak transcription	Pancreas	Pancrea
2	chr7:128117800-128163400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr7:128142200-128163200	Weak transcription	Skeletal Muscle Male	skeletal muscle
4	chr7:128153200-128163200	Weak transcription	K562	blood
5	chr7:128160600-128163200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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