Variant report

Variant	rs2937622
Chromosome Location	chr5:61045224-61045225
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs153376	1.00[ASN][1000 genomes]
rs187574	0.99[ASN][1000 genomes]
rs1979016	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2030891	0.98[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2937621	1.00[ASN][1000 genomes]
rs2937623	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2950218	0.83[EUR][1000 genomes]
rs6449548	0.80[AMR][1000 genomes]
rs7446832	0.80[AMR][1000 genomes]

No data

Chromatin state (count:4 , 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
4	chr5:61044800-61046000	Weak transcription	Brain Hippocampus Middle	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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