Variant report

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs13029758	0.81[EUR][1000 genomes]
rs1375608	0.92[EUR][1000 genomes]
rs1449483	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1449488	0.87[EUR][1000 genomes]
rs1562704	0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2290142	0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4662397	0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4662398	0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6707007	0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs72847083	0.91[EUR][1000 genomes]
rs72847089	0.91[EUR][1000 genomes]
rs72849805	0.91[EUR][1000 genomes]
rs72849811	0.91[EUR][1000 genomes]
rs72849830	0.92[EUR][1000 genomes]
rs72849836	0.92[EUR][1000 genomes]
rs72849851	0.92[EUR][1000 genomes]
rs72851456	0.92[EUR][1000 genomes]
rs72851466	0.92[EUR][1000 genomes]
rs72852610	0.84[EUR][1000 genomes]
rs72853692	0.91[EUR][1000 genomes]
rs72992499	0.84[ASN][1000 genomes]
rs72996320	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv997274	chr2:142760393-143599193	Enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv526107	chr2:142768518-142884248	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv875254	chr2:142833327-142931146	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv1006247	chr2:142851056-143289465	Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:142869400-142871600	Enhancers	Cortex derived primary cultured neurospheres	brain
2	chr2:142870000-142871400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr2:142870000-142878400	Weak transcription	Brain Hippocampus Middle	brain
4	chr2:142870200-142870800	Enhancers	Brain Anterior Caudate	brain
5	chr2:142870200-142871000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr2:142870200-142871200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr2:142870200-142871400	Enhancers	Hela-S3	cervix
8	chr2:142870600-142871200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr2:142870600-142871400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr2:142870600-142871400	Enhancers	Brain Substantia Nigra	brain

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