Variant report

Variant	rs73433293
Chromosome Location	chr15:60458440-60458441
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]
rs56756160	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57472277	1.00[AMR][1000 genomes]
rs57806408	1.00[AMR][1000 genomes]
rs58573828	1.00[AMR][1000 genomes]
rs58973920	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59297074	1.00[AMR][1000 genomes]
rs59568962	1.00[AMR][1000 genomes]
rs60051753	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61040250	1.00[AMR][1000 genomes]
rs73433211	1.00[AMR][1000 genomes]
rs73433256	1.00[AMR][1000 genomes]
rs73433284	0.80[AFR][1000 genomes]
rs73433298	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74016950	1.00[AMR][1000 genomes]
rs74016976	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	nsv904280	chr15:60042722-60524025	Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 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	chr15:60454400-60464800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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