Variant report

Variant	rs9662077
Chromosome Location	chr1:211132619-211132620
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10863871	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs11119636	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs11119639	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs1501553	0.81[AMR][1000 genomes]
rs1501561	0.80[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2088877	0.82[AMR][1000 genomes]
rs2102129	0.81[AMR][1000 genomes]
rs2202095	0.81[AMR][1000 genomes]
rs2358092	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2358117	0.85[AMR][1000 genomes]
rs4951700	0.83[AMR][1000 genomes]
rs4951701	0.83[AMR][1000 genomes]
rs6686447	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs6702809	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:211123000-211152000	Weak transcription	HSMM	muscle
2	chr1:211131600-211133000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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