Variant report

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs11793835	0.88[ASN][1000 genomes]
rs12000742	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12001739	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12003213	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12005874	0.90[EUR][1000 genomes]
rs13283809	0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1590263	0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs16931170	0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs17193016	0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs17278014	0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2065068	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2065069	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs35676237	0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs35682517	0.84[ASN][1000 genomes]
rs55932861	0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs67311478	0.85[ASN][1000 genomes]
rs7018700	0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7025155	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7025539	0.88[ASN][1000 genomes]
rs7041670	0.88[ASN][1000 genomes]
rs7869160	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1022001	chr9:13717736-13983738	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv1033764	chr9:13764918-14226168	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
3	nsv1015319	chr9:13931836-13970419	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
4	nsv613636	chr9:13936438-13975480	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
5	nsv892593	chr9:13948798-14233159	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:13962200-13969600	Weak transcription	Psoas Muscle	Psoas
2	chr9:13962400-13969600	Weak transcription	Left Ventricle	heart
3	chr9:13963600-13969800	Weak transcription	Skeletal Muscle Female	skeletal muscle
4	chr9:13967400-13970000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr9:13967800-13970200	Weak transcription	Fetal Heart	heart
6	chr9:13967800-13971400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr9:13967800-13971600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr9:13968000-13971600	Weak transcription	Fetal Lung	lung

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