Variant report

Variant	rs12789861
Chromosome Location	chr11:32360222-32360223
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs10767930	0.85[AFR][1000 genomes]
rs10835887	0.85[AFR][1000 genomes]
rs10835888	0.85[AFR][1000 genomes]
rs11031729	0.85[AFR][1000 genomes]
rs12099181	0.84[AFR][1000 genomes];0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2207548	0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2207549	0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7122775	0.85[AFR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:32356800-32364400	Weak transcription	Dnd41	blood
2	chr11:32358200-32361000	Weak transcription	Fetal Heart	heart

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

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