Variant report

Variant	rs55847434
Chromosome Location	chr8:129935087-129935088
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs13266086	0.89[AFR][1000 genomes]
rs1519846	0.88[AFR][1000 genomes]
rs1530300	0.84[AFR][1000 genomes]
rs17241908	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17242358	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs34426405	0.93[AFR][1000 genomes]
rs55658222	0.80[EUR][1000 genomes]
rs55865336	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56330003	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs72728734	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs72728736	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs987525	0.97[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:129923200-129936800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr8:129929600-129937000	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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