Variant report

Variant	rs62357177
Chromosome Location	chrX:83337758-83337759
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs16876270	0.91[EUR][1000 genomes]
rs3212394	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs41305896	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs56719416	0.86[EUR][1000 genomes]
rs62357159	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62357175	0.91[EUR][1000 genomes]
rs62357195	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs62357197	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs62357199	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs62357200	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs62357202	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs62357203	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs62357227	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs62357230	0.90[EUR][1000 genomes]
rs6450105	0.86[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:83334600-83352600	Weak transcription	Osteobl	bone
2	chrX:83337000-83337800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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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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