Variant report

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

rs_ID	r²[population]
rs1026505	0.97[ASN][1000 genomes]
rs12512152	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13112941	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1459155	0.84[ASN][1000 genomes]
rs1459156	0.90[ASN][1000 genomes]
rs17058964	0.92[ASN][1000 genomes]
rs17318218	0.83[AFR][1000 genomes];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs17318489	0.97[AFR][1000 genomes];0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1824347	0.90[ASN][1000 genomes]
rs1903126	0.97[ASN][1000 genomes]
rs1947639	0.92[ASN][1000 genomes]
rs28718496	0.90[ASN][1000 genomes]
rs34547986	0.97[AFR][1000 genomes];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs35447014	0.92[ASN][1000 genomes]
rs6553659	0.92[ASN][1000 genomes]
rs6833917	0.92[ASN][1000 genomes]
rs6844018	0.92[ASN][1000 genomes]
rs7660673	0.97[ASN][1000 genomes]
rs7673435	0.97[ASN][1000 genomes]
rs898197	0.93[ASN][1000 genomes]
rs9637709	0.97[ASN][1000 genomes]
rs9968432	0.97[AFR][1000 genomes];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[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	nsv948856	chr4:173388217-173967546	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv949126	chr4:173466221-174051451	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	esv3327952	chr4:173591786-173805861	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv881394	chr4:173757115-173847405	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:173790200-173797600	Weak transcription	iPS-18 Cell Line	embryonic stem cell

Quick Search: