Variant report

Variant	rs9548083
Chromosome Location	chr13:38433021-38433022
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs1077026	0.92[EUR][1000 genomes]
rs12583028	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12583641	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12872351	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12874874	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1415602	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1577876	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs17272200	0.82[EUR][1000 genomes]
rs2093812	0.81[EUR][1000 genomes]
rs2104326	0.81[EUR][1000 genomes]
rs34311615	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs34824702	0.81[EUR][1000 genomes]
rs35681998	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7996599	0.84[EUR][1000 genomes]
rs9532122	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs9532125	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9532126	0.81[EUR][1000 genomes]
rs9548060	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9548061	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9548064	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9548065	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9548066	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9548067	0.81[EUR][1000 genomes]
rs9548069	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9548070	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9548076	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9548077	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs9548078	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs9548079	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9548082	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9548088	0.87[AMR][1000 genomes];0.95[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	nsv915901	chr13:38199035-39032633	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
2	nsv899995	chr13:38395847-38438843	Enhancers Weak transcription ZNF genes & repeats Strong transcription	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:38423800-38435800	Weak transcription	Osteobl	bone
2	chr13:38424000-38437000	Weak transcription	Ovary	ovary
3	chr13:38432800-38435800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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