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Variant report
Variant
rs73378984
Chromosome Location
chr14:84641779-84641780
allele
C/T
Outlinks
Ensembl
 
UCSC
Chromatin state
Related regulatory elements
Target genes
Other information
TF binding region (count:0)
CpG islands (count:0)
Chromatin interactive region (count:0)
LncRNA region (count:1)
Mature miRNA region (count: 0)
miRNA target sites (count:0)
No data
No data
No data
(count:1 , 50 per page) page:
1
No.
lncRNA name
Chromosome Location
lncRNA alias
1
lnc-RP11-497E19.2.1-9
chr14:84640135-84641854
NONHSAT038102
No data
No data
No data
Extended variants information (count: 6 )
Associated traits (count: 0)
rSNPs within LD-proxies of this variant (count:4)
rs_ID
r
2
[population]
rs41519447
1.00[AMR][1000 genomes]
rs59321128
1.00[AMR][1000 genomes]
rs73365597
1.00[AMR][1000 genomes]
rs73367231
1.00[AMR][1000 genomes]
Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page:
1
No.
Variant name
Chromosome position
Chromatin state
Related regulatory elements
Target genes
Extended variants
Associated traits
1
nsv565376
chr14:84612088-84644822
Enhancers Weak transcription
TF binding regionlncRNA
3 gene(s)
inside rSNPs
diseases
2
nsv983846
chr14:84641622-84643399
Inactive region
lncRNA
n/a
inside rSNPs
n/a
No data
Chromatin state (count:0 , 50 per page) page:
No data
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
New variant types
New dimension of annotation
New regulatory manner
More detailed annotation on variant overlapped TFBS
More extended data
New search manner
Quick links