Variant report

Variant	rs7001883
Chromosome Location	chr8:54369872-54369873
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs10088812	0.88[ASN][1000 genomes]
rs10089658	0.98[ASN][1000 genomes]
rs10101861	0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10103617	0.88[ASN][1000 genomes]
rs10105375	0.87[ASN][1000 genomes]
rs10216984	0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10958358	0.87[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10958365	0.98[ASN][1000 genomes]
rs10958367	0.88[ASN][1000 genomes]
rs10958368	0.87[ASN][1000 genomes]
rs12235032	0.87[ASN][1000 genomes]
rs12542325	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12544025	0.88[ASN][1000 genomes]
rs12546500	0.88[ASN][1000 genomes]
rs13251975	0.88[ASN][1000 genomes]
rs13262157	0.98[ASN][1000 genomes]
rs13265261	0.88[ASN][1000 genomes]
rs1351064	0.90[ASN][1000 genomes]
rs1351065	0.80[ASN][1000 genomes]
rs1477948	0.87[ASN][1000 genomes]
rs1477971	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1477973	0.87[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1477977	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1477978	0.88[ASN][1000 genomes]
rs1477980	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1551915	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2376147	0.86[ASN][1000 genomes]
rs4581080	0.86[EUR][1000 genomes]
rs6473825	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6473826	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6982097	0.91[ASN][1000 genomes]
rs6989685	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6993966	0.87[AFR][1000 genomes];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7007299	0.92[AFR][1000 genomes];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7835893	0.96[ASN][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	esv3377304	chr8:53873441-54380875	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	esv2752674	chr8:54181147-54483747	Flanking Active TSS Weak transcription Active TSS Enhancers ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	esv3407557	chr8:54348448-54395357	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers	lncRNA	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	chr8:54367400-54372000	Weak transcription	Fetal Heart	heart

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