Variant report

Variant	rs2937623
Chromosome Location	chr5:61044410-61044411
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs153376	1.00[ASN][1000 genomes]
rs187574	0.99[ASN][1000 genomes]
rs1979016	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2030891	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2937621	1.00[ASN][1000 genomes]
rs2937622	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2950218	0.90[EUR][1000 genomes]
rs6449548	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7446832	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7447792	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:61034000-61073400	Weak transcription	Brain Substantia Nigra	brain
2	chr5:61034600-61046000	Weak transcription	Brain Cingulate Gyrus	brain
3	chr5:61044000-61046400	Weak transcription	Brain Inferior Temporal Lobe	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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