Variant report

Variant	rs73272630
Chromosome Location	chr14:65576201-65576202
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]
rs2296314	0.85[ASN][1000 genomes]
rs2296320	0.85[ASN][1000 genomes]
rs34601568	1.00[ASN][1000 genomes]
rs3783716	0.95[ASN][1000 genomes]
rs3783717	0.95[ASN][1000 genomes]
rs3783718	0.95[ASN][1000 genomes]
rs3783719	0.95[ASN][1000 genomes]
rs3825641	1.00[ASN][1000 genomes]
rs56325087	0.95[ASN][1000 genomes]
rs7142375	1.00[ASN][1000 genomes]
rs7155468	0.95[ASN][1000 genomes]
rs72728236	0.95[ASN][1000 genomes]
rs9944027	1.00[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	nsv832816	chr14:65473244-65644645	Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	19 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	chr14:65575600-65577600	Enhancers	K562	blood
2	chr14:65576000-65576400	Enhancers	Fetal Thymus	thymus

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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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