Variant report

Variant	rs73574428
Chromosome Location	chr6:142608528-142608529
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs55804427	0.83[AMR][1000 genomes]
rs59792272	0.96[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs73574424	0.85[AMR][1000 genomes]
rs73574429	0.85[AMR][1000 genomes]
rs9484608	0.83[AMR][1000 genomes]
rs9484611	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs9484614	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs9496311	0.83[AMR][1000 genomes]
rs9496315	0.83[AMR][1000 genomes]
rs9496316	0.91[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs9496319	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs9496320	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs9496323	0.85[AMR][1000 genomes]
rs9496324	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9496325	0.85[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949088	chr6:142561402-143128849	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	nsv830825	chr6:142585242-142752575	Enhancers Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv1029666	chr6:142594099-142643084	Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 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	chr6:142607400-142612200	Weak transcription	A549	lung
2	chr6:142608000-142610400	Weak transcription	HepG2	liver

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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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