Variant report

Variant	rs7792642
Chromosome Location	chr7:103601362-103601363
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10237086	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1123034	0.81[EUR][1000 genomes]
rs4236564	0.84[EUR][1000 genomes]
rs4236565	0.84[EUR][1000 genomes]
rs4236566	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4259349	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4291202	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4424197	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4425676	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4460305	0.81[JPT][hapmap];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4473962	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4475416	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4483088	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4621738	0.81[JPT][hapmap];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4636135	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4727579	0.84[EUR][1000 genomes]
rs6465948	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6950228	0.80[JPT][hapmap];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6957898	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6966767	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6967972	0.81[EUR][1000 genomes]
rs6971036	0.81[JPT][hapmap];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6971140	0.81[JPT][hapmap];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6971418	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6976042	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7782058	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7785983	0.81[JPT][hapmap];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7787670	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7787675	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9632691	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9918509	0.89[AMR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:103598200-103602800	Weak transcription	Fetal Heart	heart
2	chr7:103599000-103604200	Weak transcription	K562	blood
3	chr7:103599000-103607800	Weak transcription	HepG2	liver

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