Variant report

Variant	rs12548216
Chromosome Location	chr8:129814716-129814717
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs12541508	0.93[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs12544345	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12548853	0.84[AMR][1000 genomes]
rs12549751	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs13269648	0.86[AFR][1000 genomes];0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs34093858	0.82[EUR][1000 genomes]
rs34757177	0.93[AFR][1000 genomes];0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs35697214	0.82[EUR][1000 genomes]
rs36040241	0.82[EUR][1000 genomes]
rs36142507	0.93[AFR][1000 genomes];0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs67628488	0.93[AFR][1000 genomes];0.84[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	chr8:129807000-129820800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr8:129813600-129819800	Weak transcription	Dnd41	blood

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Input of quick search could be:

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

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