Variant report

Variant	rs74016649
Chromosome Location	chr15:54818475-54818476
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:13)

rs_ID	r²[population]
rs16974701	0.83[ASN][1000 genomes]
rs16974744	1.00[AMR][1000 genomes]
rs57288219	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57409526	1.00[EUR][1000 genomes]
rs61120383	1.00[EUR][1000 genomes]
rs61283136	0.95[ASN][1000 genomes]
rs7180034	0.86[ASN][1000 genomes]
rs74014207	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74014210	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74014212	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74016655	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74016656	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8026071	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv817539	chr15:54132584-55095235	Weak transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	nsv1038660	chr15:54756184-55039913	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 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	chr15:54807000-54820600	Weak transcription	Fetal Brain Male	brain
2	chr15:54811000-54869600	Weak transcription	Aorta	Aorta
3	chr15:54818400-54825600	Weak transcription	Fetal Lung	lung

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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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