Variant report

Variant	rs72619135
Chromosome Location	chr4:18627612-18627613
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs16897260	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs16897267	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17483640	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17483809	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17548590	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17549164	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2320734	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4057148	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4274839	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4543111	0.81[EUR][1000 genomes]
rs55733109	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56743640	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57400503	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59434531	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60238011	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66464677	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66526344	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs66818344	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6812709	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72619128	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72619129	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72619130	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72619136	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72619137	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73098395	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7679250	0.81[AFR][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	nsv1003931	chr4:18241575-18849898	Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv533087	chr4:18362040-19176896	Enhancers Bivalent Enhancer ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv532708	chr4:18596861-19176896	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:18627200-18628200	Enhancers	Fetal Brain Male	brain
2	chr4:18627600-18630800	Weak transcription	Placenta	Placenta

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