Variant report

Variant	rs61117837
Chromosome Location	chr11:74850240-74850241
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs11827488	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12281823	0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12361277	0.93[ASN][1000 genomes]
rs17133732	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4100076	0.87[ASN][1000 genomes]
rs4944072	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4944073	0.81[ASN][1000 genomes]
rs4944974	0.87[ASN][1000 genomes]
rs4944993	0.81[ASN][1000 genomes]
rs55986601	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs58626404	0.90[ASN][1000 genomes]
rs6592602	0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs66687047	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs67904312	0.81[ASN][1000 genomes]
rs67947132	0.93[ASN][1000 genomes]
rs7122309	0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72996586	0.93[ASN][1000 genomes]

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:74842000-74851400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr11:74846600-74851400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr11:74846600-74853800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr11:74847000-74853800	Weak transcription	Adipose Nuclei	Adipose
5	chr11:74847200-74852400	Weak transcription	K562	blood
6	chr11:74848400-74851400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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