Variant report

Variant	rs74030511
Chromosome Location	chr15:92823524-92823525
allele	C/T
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:14)

rs_ID	r²[population]
rs55937656	1.00[AMR][1000 genomes]
rs60855340	1.00[AMR][1000 genomes]
rs74028809	1.00[AMR][1000 genomes]
rs74028810	1.00[AMR][1000 genomes]
rs74028819	1.00[AMR][1000 genomes]
rs74028823	1.00[AMR][1000 genomes]
rs74028831	1.00[AMR][1000 genomes]
rs74028833	1.00[AMR][1000 genomes]
rs74028883	1.00[AMR][1000 genomes]
rs74028892	1.00[AMR][1000 genomes]
rs74030509	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74030510	1.00[AMR][1000 genomes]
rs74030520	1.00[AMR][1000 genomes]
rs74030524	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948621	chr15:92688981-93158095	Enhancers Bivalent/Poised TSS ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
2	nsv1049561	chr15:92758434-93097965	Enhancers Weak transcription Bivalent/Poised TSS Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
3	nsv1037972	chr15:92804908-93270761	Flanking Bivalent TSS/Enh Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:92822400-92823800	Enhancers	Liver	Liver
2	chr15:92822600-92823600	Enhancers	Fetal Stomach	stomach
3	chr15:92823400-92823800	Enhancers	Ovary	ovary
4	chr15:92823400-92824200	Enhancers	Rectal Smooth Muscle	rectum

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