Variant report

Variant	rs16844177
Chromosome Location	chr2:141293697-141293698
allele	A/C
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]
rs16844161	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16844168	0.83[EUR][1000 genomes]
rs16844171	0.83[EUR][1000 genomes]
rs16844174	0.83[EUR][1000 genomes]
rs16844178	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16844181	0.89[AFR][1000 genomes];0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs16844186	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs16844189	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs16844198	0.89[AFR][1000 genomes];0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs16844202	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16844206	0.89[AFR][1000 genomes];0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs16844234	0.83[AMR][1000 genomes]
rs16844252	0.95[EUR][1000 genomes]
rs16844253	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs17591870	0.83[AMR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:141287600-141297200	Weak transcription	Brain Substantia Nigra	brain

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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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