Variant report

Variant	rs73944973
Chromosome Location	chr18:25210947-25210948
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs56774619	1.00[ASN][1000 genomes]
rs59085826	1.00[AFR][1000 genomes]
rs59993739	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs61020210	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs73396752	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs73396756	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs73396787	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs73412987	1.00[AFR][1000 genomes]
rs73413000	1.00[AFR][1000 genomes]
rs73414911	1.00[AFR][1000 genomes]
rs73414945	1.00[AFR][1000 genomes]
rs73414946	1.00[AFR][1000 genomes]
rs9946894	0.89[ASN][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	esv2761996	chr18:24866083-25818618	Flanking Active TSS Enhancers Strong transcription Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 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	chr18:25210800-25211200	Enhancers	Placenta Amnion	Placenta Amnion

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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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