Variant report

Variant	rs72951797
Chromosome Location	chr4:150206580-150206581
allele	A/C
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:21)

rs_ID	r²[population]
rs4301085	1.00[AMR][1000 genomes]
rs4510455	1.00[AMR][1000 genomes]
rs59690219	1.00[AMR][1000 genomes]
rs61133328	1.00[AMR][1000 genomes]
rs72951771	1.00[AMR][1000 genomes]
rs72951795	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]
rs72966027	1.00[AMR][1000 genomes]
rs72966028	1.00[AMR][1000 genomes]
rs72966031	1.00[AMR][1000 genomes]
rs72966091	1.00[AMR][1000 genomes]
rs72966101	1.00[AMR][1000 genomes]
rs72967931	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	nsv880249	chr4:150156579-150280221	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv1016977	chr4:150173255-150605595	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv537298	chr4:150173255-150605595	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 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	chr4:150202800-150207600	Weak transcription	Fetal Lung	lung

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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

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