Variant report

Variant	rs12264531
Chromosome Location	chr10:93291747-93291748
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]
rs10128490	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11186599	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11186600	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11186601	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11186603	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs17106727	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7076439	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7079061	0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:93272200-93296000	Weak transcription	HSMMtube	muscle
2	chr10:93278200-93296000	Weak transcription	HSMM	muscle
3	chr10:93278400-93298400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr10:93288600-93296000	Weak transcription	Right Atrium	heart
5	chr10:93289400-93296000	Weak transcription	Liver	Liver
6	chr10:93289600-93296000	Weak transcription	Aorta	Aorta
7	chr10:93290000-93296000	Weak transcription	Pancreas	Pancrea
8	chr10:93290000-93296200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
9	chr10:93290800-93297000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin

Quick Search:

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

what's new

Quick links