Variant report

Variant	rs4726755
Chromosome Location	chr7:145021305-145021306
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs1002527	0.85[ASN][1000 genomes]
rs10255844	0.89[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10271795	0.99[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10952614	0.97[ASN][1000 genomes]
rs10952616	0.97[ASN][1000 genomes]
rs11765651	0.89[ASN][1000 genomes]
rs11976907	0.97[ASN][1000 genomes]
rs12112673	0.97[ASN][1000 genomes]
rs12112682	0.81[ASN][1000 genomes]
rs12673814	0.85[ASN][1000 genomes]
rs1468374	0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1468375	0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17805910	0.97[ASN][1000 genomes]
rs17806163	0.95[ASN][1000 genomes]
rs1859565	0.88[ASN][1000 genomes]
rs2023995	0.87[ASN][1000 genomes]
rs2107891	0.89[ASN][1000 genomes]
rs2190081	0.94[ASN][1000 genomes]
rs2371963	0.89[ASN][1000 genomes]
rs4726756	0.97[ASN][1000 genomes]
rs4726758	0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57132884	0.97[ASN][1000 genomes]
rs57524854	0.96[ASN][1000 genomes]
rs59098873	0.97[ASN][1000 genomes]
rs62495645	0.96[ASN][1000 genomes]
rs62495646	0.96[ASN][1000 genomes]
rs62495647	0.96[ASN][1000 genomes]
rs62495920	0.97[ASN][1000 genomes]
rs62495921	0.97[ASN][1000 genomes]
rs62495922	0.97[ASN][1000 genomes]
rs62495923	0.97[ASN][1000 genomes]
rs6464672	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs67346243	0.97[ASN][1000 genomes]
rs6972400	0.97[ASN][1000 genomes]
rs7779709	0.85[ASN][1000 genomes]
rs7779731	0.87[ASN][1000 genomes]
rs7780174	0.86[ASN][1000 genomes]
rs7780968	0.89[ASN][1000 genomes]
rs7790233	0.88[ASN][1000 genomes]
rs7792751	0.81[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7799717	0.86[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	nsv1031071	chr7:144318082-145125392	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
2	nsv539169	chr7:144318082-145125392	Weak transcription Flanking Active TSS Active TSS Enhancers Bivalent/Poised TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
3	esv3401346	chr7:145018769-145021517	ZNF genes & repeats Enhancers	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:145021000-145021600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr7:145021200-145021600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr7:145021200-145021600	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr7:145021200-145021600	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr7:145021200-145021600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr7:145021200-145021600	ZNF genes & repeats	Gastric	stomach
7	chr7:145021200-145021600	ZNF genes & repeats	Pancreas	Pancrea

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