Variant report

Variant	rs74120203
Chromosome Location	chr10:18356898-18356899
allele	A/G
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]
rs11813889	0.88[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11817171	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16916829	0.91[AFR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16916837	1.00[ASN][1000 genomes]
rs58142633	0.92[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7067765	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7090868	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74118097	0.91[AFR][1000 genomes]
rs74118099	0.91[AFR][1000 genomes]
rs74118101	0.81[AFR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:18349200-18359200	Weak transcription	Stomach Smooth Muscle	stomach
2	chr10:18356400-18359400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr10:18356400-18359600	Weak transcription	NHEK	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