Variant report

Variant	rs73901582
Chromosome Location	chr20:23039663-23039664
allele	A/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]
rs1331081	1.00[AMR][1000 genomes]
rs1537133	1.00[AMR][1000 genomes]
rs55783247	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs55964438	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56978650	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57610255	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59053572	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7266993	1.00[AMR][1000 genomes]
rs73901579	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73901583	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73901586	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73901588	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73901589	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73901591	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8123988	1.00[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	nsv912816	chr20:22757960-23062927	Flanking Active TSS Bivalent/Poised TSS Enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	esv2758516	chr20:23029404-23173240	Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
3	esv2758789	chr20:23029404-23179604	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:23032600-23041800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr20:23032800-23041400	Weak transcription	Spleen	Spleen
3	chr20:23033400-23040200	Weak transcription	Placenta	Placenta
4	chr20:23038400-23046600	Enhancers	Fetal Lung	lung
5	chr20:23039600-23043400	Enhancers	Dnd41	blood

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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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