Variant report

Variant	rs9964481
Chromosome Location	chr18:44103321-44103322
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]
rs12456713	0.92[ASN][1000 genomes]
rs12606812	0.85[AFR][1000 genomes];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4890330	0.92[ASN][1000 genomes]
rs4890667	0.85[CEU][hapmap];0.95[YRI][hapmap];0.92[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs986117	0.86[JPT][hapmap]
rs9949102	0.91[YRI][hapmap]
rs9951898	0.90[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs9962885	0.80[AMR][1000 genomes];0.83[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:44086000-44114400	Weak transcription	Spleen	Spleen
2	chr18:44093200-44118600	Strong transcription	Primary monocytes fromperipheralblood	blood
3	chr18:44093200-44120400	Strong transcription	Primary neutrophils fromperipheralblood	blood
4	chr18:44094000-44126000	Weak transcription	Adipose Nuclei	Adipose
5	chr18:44098800-44107800	Strong transcription	Monocytes-CD14+_RO01746	blood
6	chr18:44101400-44104400	Weak transcription	Lung	lung

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