Variant report

Variant	rs12564959
Chromosome Location	chr1:86484560-86484561
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:86483581..86486265-chr1:86488492..86490836,2	K562	blood:

Extended variants
information (count: 50 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs10493787	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10493788	0.88[ASN][1000 genomes]
rs11583563	0.80[ASN][1000 genomes]
rs11588997	0.80[ASN][1000 genomes]
rs12402809	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12408108	0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12566718	0.83[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12566940	0.83[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12567495	0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12567549	0.89[EUR][1000 genomes]
rs12744313	0.80[ASN][1000 genomes]
rs12753548	0.80[ASN][1000 genomes]
rs12754154	0.80[ASN][1000 genomes]
rs1408667	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1408668	0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs17405393	0.80[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs17406450	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs17406471	0.88[EUR][1000 genomes]
rs17406755	0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs17414470	0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs17415366	0.88[EUR][1000 genomes]
rs41313268	0.80[ASN][1000 genomes]
rs4912460	0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs517786	0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs540159	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs565860	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs569541	0.88[ASN][1000 genomes]
rs61783511	0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs61800687	0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs61800722	0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs61800724	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs61800727	0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs61800729	0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs61800732	0.91[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs61800734	0.87[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs61802172	0.82[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs629683	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs645271	0.88[ASN][1000 genomes]
rs6665582	0.80[ASN][1000 genomes]
rs72716135	0.93[EUR][1000 genomes]
rs72716141	0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs72716150	0.87[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs72716152	0.87[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7414042	0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7548696	0.80[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	nsv817212	chr1:86127851-86658426	Enhancers Weak transcription Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv546722	chr1:86278315-86891073	Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	9 gene(s)	inside rSNPs	diseases
3	nsv462406	chr1:86412177-86509996	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv546757	chr1:86412177-86509996	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv1010312	chr1:86469730-86686426	Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs12564959	COL24A1	cis	Artery Tibial	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:86482200-86487600	Weak transcription	Fetal Lung	lung
2	chr1:86483600-86484600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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