Variant report

Variant	rs72967931
Chromosome Location	chr4:150119801-150119802
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs59690219	1.00[AMR][1000 genomes]
rs61133328	1.00[AMR][1000 genomes]
rs72951771	1.00[AMR][1000 genomes]
rs72951795	1.00[AMR][1000 genomes]
rs72951797	1.00[AMR][1000 genomes]
rs72953611	1.00[AMR][1000 genomes]
rs72953613	1.00[AMR][1000 genomes]
rs72953615	1.00[AMR][1000 genomes]
rs72953627	1.00[AMR][1000 genomes]
rs72953659	1.00[AMR][1000 genomes]
rs72953662	1.00[AMR][1000 genomes]
rs72953666	1.00[AMR][1000 genomes]
rs72953668	1.00[AMR][1000 genomes]
rs72953669	1.00[AMR][1000 genomes]
rs72963932	1.00[AMR][1000 genomes]
rs72966027	1.00[AMR][1000 genomes]
rs72966028	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72966031	1.00[AMR][1000 genomes]
rs72966091	1.00[AMR][1000 genomes]
rs72966101	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	nsv880247	chr4:150057979-150159936	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv1022438	chr4:150066349-150196711	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv595687	chr4:150070596-150178533	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv880248	chr4:150092178-150200706	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:150117400-150122600	Weak transcription	Fetal Heart	heart

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