Variant report

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10064404	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10066485	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10072474	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10074079	0.91[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13436904	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs13436919	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes]
rs4274943	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes]
rs4355479	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes]
rs4380600	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes]
rs4425466	0.90[CEU][hapmap]
rs4472223	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs4498222	0.80[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4526067	0.84[AMR][1000 genomes]
rs4572962	0.80[CEU][hapmap]
rs55728436	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs55944106	0.93[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs56145198	0.89[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs56298453	0.81[AMR][1000 genomes]
rs57059470	0.80[AFR][1000 genomes]
rs57348772	0.84[AMR][1000 genomes]
rs60775366	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes]
rs6450249	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes]
rs66812968	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs6876730	0.84[AMR][1000 genomes]
rs72757444	0.80[EUR][1000 genomes]
rs7703792	0.84[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7734384	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 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
3	esv3358092	chr5:54077828-54189150	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	esv2754136	chr5:54083387-54107727	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:54073000-54097600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr5:54081400-54083600	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr5:54082000-54088600	Weak transcription	Fetal Stomach	stomach
4	chr5:54082400-54087600	Weak transcription	Fetal Muscle Trunk	muscle
5	chr5:54083200-54083600	Enhancers	Monocytes-CD14+_RO01746	blood
6	chr5:54083200-54084400	Weak transcription	Left Ventricle	heart
7	chr5:54083200-54088000	Weak transcription	Fetal Heart	heart
8	chr5:54083200-54088800	Weak transcription	Aorta	Aorta
9	chr5:54083400-54087400	Weak transcription	Fetal Muscle Leg	muscle

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