Variant report

Variant	rs73615218
Chromosome Location	chr13:110595731-110595732
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs10161700	1.00[AMR][1000 genomes]
rs12017337	1.00[AMR][1000 genomes]
rs28516927	1.00[AMR][1000 genomes]
rs57456074	1.00[EUR][1000 genomes]
rs60144751	1.00[AMR][1000 genomes]
rs7358943	1.00[AMR][1000 genomes]
rs74124147	1.00[AMR][1000 genomes]
rs7989379	1.00[EUR][1000 genomes]
rs9587981	1.00[AMR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832719	chr13:110512259-110655883	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:110591400-110596400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr13:110594600-110597400	Weak transcription	Muscle Satellite Cultured Cells	--
3	chr13:110595200-110597400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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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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