Variant report

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

rs_ID	r²[population]
rs10506195	0.84[CEU][hapmap];0.89[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11615166	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12811069	0.84[CEU][hapmap];0.89[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12822018	0.81[EUR][1000 genomes]
rs12823312	0.85[CEU][hapmap];0.89[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1379779	0.85[CEU][hapmap];0.89[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs17129392	0.80[CEU][hapmap]
rs17129427	0.84[CEU][hapmap];0.84[EUR][1000 genomes]
rs17578886	0.90[CEU][hapmap];0.85[EUR][1000 genomes]
rs17768388	0.89[CEU][hapmap];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1902905	0.81[EUR][1000 genomes]
rs34298736	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs34607783	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs35002976	0.86[EUR][1000 genomes]
rs35032376	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs35667109	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs35753665	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs36020206	0.88[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs36038624	0.81[EUR][1000 genomes]
rs57639356	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs58667777	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs67541586	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs71451530	0.83[EUR][1000 genomes]
rs7957589	0.80[EUR][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	nsv832384	chr12:41772648-41971430	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	esv3337301	chr12:41851654-42093677	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv899040	chr12:41905897-42181706	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:41925600-41949800	Weak transcription	Stomach Smooth Muscle	stomach
2	chr12:41925800-41944800	Weak transcription	Brain Germinal Matrix	brain
3	chr12:41942800-41956800	Weak transcription	Colon Smooth Muscle	Colon

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