Variant report

Variant	rs73893205
Chromosome Location	chr21:17518789-17518790
allele	A/T
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:13)

rs_ID	r²[population]
rs10222055	1.00[EUR][1000 genomes]
rs28424182	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28886124	1.00[EUR][1000 genomes]
rs58748147	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61645626	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73367165	1.00[EUR][1000 genomes]
rs7349006	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73893207	1.00[EUR][1000 genomes]
rs9808767	1.00[EUR][1000 genomes]
rs9974231	1.00[EUR][1000 genomes]
rs9976336	1.00[EUR][1000 genomes]
rs9984291	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9985009	0.81[AMR][1000 genomes];1.00[EUR][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	nsv1066951	chr21:17458978-17603160	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv544381	chr21:17458978-17603160	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	esv3398505	chr21:17499130-17527355	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Genic enhancers Active TSS	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:1 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:17518200-17526800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured 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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