Variant report

Variant	rs2602655
Chromosome Location	chr2:125669260-125669261
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10165689	0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10189275	0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11891962	0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11894518	0.85[EUR][1000 genomes]
rs11898056	0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1340187	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1361439	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs17637918	0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs17637939	0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1840202	0.92[ASN][1000 genomes]
rs1840206	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1840207	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2068359	0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2249026	0.89[EUR][1000 genomes]
rs2602644	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2602645	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2602646	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2791629	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2791631	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs58560012	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs62173301	0.92[ASN][1000 genomes]
rs6541974	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6716082	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6721641	0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv834360	chr2:125492685-125683200	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv834361	chr2:125601081-125810992	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:125668600-125670000	Enhancers	Brain Hippocampus Middle	brain
2	chr2:125668800-125669800	Enhancers	Brain Substantia Nigra	brain
3	chr2:125668800-125670000	Enhancers	Brain Cingulate Gyrus	brain
4	chr2:125669000-125670200	Enhancers	Fetal Stomach	stomach

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