Variant report

Variant	rs73786405
Chromosome Location	chr5:116341428-116341429
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs1350575	0.82[EUR][1000 genomes]
rs1350577	1.00[EUR][1000 genomes]
rs57780571	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58275123	0.90[EUR][1000 genomes]
rs6878581	0.90[EUR][1000 genomes]
rs73254902	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs73256904	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs73268804	1.00[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs73782990	1.00[EUR][1000 genomes]
rs73782997	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73782999	0.83[AMR][1000 genomes];1.00[EUR][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	nsv1020292	chr5:116183712-116349633	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv1033379	chr5:116244963-116464338	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv1016586	chr5:116317968-116377074	Weak transcription ZNF genes & repeats Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv1028067	chr5:116340955-116427869	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 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	chr5:116340600-116341600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
2	chr5:116341000-116341600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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