Variant report

Variant	rs55658222
Chromosome Location	chr8:129976136-129976137
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs17241908	0.80[EUR][1000 genomes]
rs17242358	0.95[AFR][1000 genomes];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55847434	0.80[EUR][1000 genomes]
rs55865336	0.80[EUR][1000 genomes]
rs7017665	0.95[EUR][1000 genomes]
rs72728734	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs72728736	0.80[EUR][1000 genomes]
rs72728755	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:129970800-129982400	Weak transcription	HSMM	muscle
2	chr8:129973000-129976600	Weak transcription	Dnd41	blood

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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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