Variant report

Variant	rs73850662
Chromosome Location	chr4:143969387-143969388
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs55675363	1.00[AMR][1000 genomes]
rs56307609	1.00[AFR][1000 genomes]
rs58070744	1.00[AMR][1000 genomes]
rs58306079	1.00[AMR][1000 genomes]
rs58701532	1.00[AMR][1000 genomes]
rs59191273	1.00[AFR][1000 genomes]
rs60285299	1.00[AMR][1000 genomes]
rs60299762	0.90[AFR][1000 genomes]
rs60387330	1.00[AMR][1000 genomes]
rs61538113	1.00[AMR][1000 genomes]
rs61741556	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73850587	1.00[AMR][1000 genomes]
rs73850588	1.00[AMR][1000 genomes]
rs73850592	1.00[AMR][1000 genomes]
rs73850620	1.00[AMR][1000 genomes]
rs73850621	1.00[AMR][1000 genomes]
rs73850622	1.00[AMR][1000 genomes]
rs73850641	1.00[AMR][1000 genomes]
rs73850666	1.00[AFR][1000 genomes]
rs73850667	1.00[AFR][1000 genomes]
rs73853610	1.00[AMR][1000 genomes]
rs7654096	1.00[AMR][1000 genomes]
rs7668584	1.00[AMR][1000 genomes]
rs7690525	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1033285	chr4:143884298-144010784	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	n/a
2	nsv537288	chr4:143884298-144010784	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	n/a
3	nsv880176	chr4:143929235-144027729	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv1034895	chr4:143945139-144079655	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:143968000-143970600	Weak transcription	Brain Cingulate Gyrus	brain
2	chr4:143968200-143970600	Weak transcription	Fetal Intestine Small	intestine

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