Variant report

Variant	rs55728436
Chromosome Location	chr5:54074720-54074721
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs10064404	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs10066485	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs10072474	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs10074079	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs10075754	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs13436904	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs13436919	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs17346285	0.84[AFR][1000 genomes];0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2121130	0.83[EUR][1000 genomes]
rs2166355	0.84[EUR][1000 genomes]
rs35463987	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4274943	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4301189	0.80[EUR][1000 genomes]
rs4355479	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4380600	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4425466	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4472223	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs4526067	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs4572962	0.90[EUR][1000 genomes]
rs55944106	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs56145198	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs56202300	0.83[AFR][1000 genomes];0.88[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs56207018	0.89[EUR][1000 genomes]
rs56298453	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs56386053	0.83[AFR][1000 genomes];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs57059470	0.96[EUR][1000 genomes]
rs57348772	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs60775366	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6450249	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs66533726	0.85[EUR][1000 genomes]
rs66599423	0.85[EUR][1000 genomes]
rs66812968	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs66955270	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs67510332	0.84[EUR][1000 genomes]
rs6867643	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs6876730	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6897534	0.83[EUR][1000 genomes]
rs72757444	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs72757446	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs72760107	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7703792	0.81[AMR][1000 genomes]
rs7710436	0.89[EUR][1000 genomes]
rs7733091	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7734384	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv880717	chr5:54025701-54106378	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv830300	chr5:54056300-54257344	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:54068400-54074800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr5:54071400-54080800	Weak transcription	Primary B cells from cord blood	blood
3	chr5:54072800-54074800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr5:54073000-54097600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr5:54073400-54074800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr5:54074000-54075000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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