Variant report

Variant	rs38209
Chromosome Location	chr7:15914461-15914462
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 38 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs10226196	0.90[CHB][hapmap]
rs10253795	0.85[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs10486782	0.90[CHB][hapmap]
rs12699757	0.88[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs1298311	0.83[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs38183	0.81[AMR][1000 genomes]
rs38184	0.81[AMR][1000 genomes]
rs38185	0.81[AMR][1000 genomes]
rs38187	0.81[AMR][1000 genomes]
rs38199	0.81[AMR][1000 genomes]
rs38200	0.81[AMR][1000 genomes]
rs38202	0.82[AMR][1000 genomes]
rs38208	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs38220	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs38222	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs38223	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs38224	0.88[AMR][1000 genomes]
rs38226	0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs38231	0.94[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs38233	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs38234	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs38236	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs38238	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs38239	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs38251	0.84[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs38252	0.83[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs38258	0.84[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs6949049	0.83[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs6959942	0.80[AMR][1000 genomes]
rs6962520	0.85[AMR][1000 genomes]
rs6965426	0.84[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs6970657	0.84[AMR][1000 genomes]
rs768667	0.84[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs800713	0.85[AMR][1000 genomes]
rs800715	0.84[AMR][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	nsv523199	chr7:15582208-16042596	Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
2	nsv1016642	chr7:15884061-16799788	Genic enhancers Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
3	nsv1017958	chr7:15910153-15956470	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs38209	ANKMY2	cis	cerebellum	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:15914000-15915000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr7:15914200-15914800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr7:15914400-15914800	Enhancers	Fetal Lung	lung

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