Variant report

Variant	rs73183722
Chromosome Location	chr12:104795547-104795548
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs10861216	0.83[EUR][1000 genomes]
rs12425334	0.83[EUR][1000 genomes]
rs12425523	0.83[EUR][1000 genomes]
rs17035504	0.81[EUR][1000 genomes]
rs17035521	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17202862	0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1922264	0.83[EUR][1000 genomes]
rs3935020	0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4403872	0.83[EUR][1000 genomes]
rs57710522	0.81[EUR][1000 genomes]
rs60394569	0.81[EUR][1000 genomes]
rs73181944	0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73183716	0.81[EUR][1000 genomes]
rs73183723	0.83[EUR][1000 genomes]
rs7486552	0.81[EUR][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	nsv899494	chr12:104561521-104806232	Flanking Active TSS Weak transcription Genic enhancers Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 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	chr12:104778200-104801400	Weak transcription	A549	lung
2	chr12:104794600-104795800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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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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