Variant report

Variant	rs28497808
Chromosome Location	chr9:96578158-96578159
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs10992822	1.00[EUR][1000 genomes]
rs1123475	1.00[EUR][1000 genomes]
rs12350884	0.83[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs28369450	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs28591208	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs28848910	0.83[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs58747030	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs61281791	1.00[EUR][1000 genomes]
rs61301026	1.00[EUR][1000 genomes]
rs7021423	1.00[EUR][1000 genomes]
rs7848429	1.00[EUR][1000 genomes]
rs7850596	1.00[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:96577200-96581600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr9:96577800-96578400	Bivalent Enhancer	Fetal Stomach	stomach

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