Variant report

Variant	rs13058224
Chromosome Location	chr22:30247995-30247996
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	chr22:30238896..30240450-chr22:30246132..30247997,2	K562	blood:

Extended variants
information (count: 56 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs12484010	0.95[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs12484420	0.81[AMR][1000 genomes]
rs13053389	0.85[AMR][1000 genomes]
rs13055998	0.81[AMR][1000 genomes]
rs13058334	0.83[AMR][1000 genomes]
rs16988123	0.81[AMR][1000 genomes]
rs16988145	0.81[AMR][1000 genomes]
rs1894472	0.84[AMR][1000 genomes]
rs34955393	0.82[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs35361418	0.85[AMR][1000 genomes]
rs3788422	0.81[AMR][1000 genomes]
rs4343558	0.95[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs4820821	0.82[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs4820825	0.81[AMR][1000 genomes]
rs4823056	0.93[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs4823057	0.82[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs4823058	0.93[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs4823064	0.85[AMR][1000 genomes]
rs55686007	0.90[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs5752969	0.88[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs5752976	0.85[AMR][1000 genomes]
rs5752997	0.81[AMR][1000 genomes]
rs5763543	0.93[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs5763544	0.93[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs5763552	0.95[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs5763553	0.95[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs5763556	0.83[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs5763557	0.84[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs5763561	0.90[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs5763566	0.90[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs5763569	0.90[AMR][1000 genomes]
rs5763575	0.81[AMR][1000 genomes]
rs5763585	0.85[AMR][1000 genomes]
rs5763601	0.81[AMR][1000 genomes]
rs5763602	0.85[AMR][1000 genomes]
rs5763604	0.85[AMR][1000 genomes]
rs5763606	0.85[AMR][1000 genomes]
rs5763609	0.85[AMR][1000 genomes]
rs5763629	0.81[AMR][1000 genomes]
rs5763637	0.81[AMR][1000 genomes]
rs5763648	0.81[AMR][1000 genomes]
rs5763681	0.81[AMR][1000 genomes]
rs5763687	0.81[AMR][1000 genomes]
rs5763695	0.81[AMR][1000 genomes]
rs5763701	0.81[AMR][1000 genomes]
rs5997542	0.82[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs6006278	0.82[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs71331220	0.81[AMR][1000 genomes]
rs7292355	0.93[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs8138404	0.81[AMR][1000 genomes]
rs916807	0.81[AMR][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	nsv529742	chr22:29677909-30274388	Bivalent Enhancer Enhancers ZNF genes & repeats Strong transcription Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
2	nsv1064081	chr22:29826745-30623965	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
3	nsv544677	chr22:29826745-30623965	Weak transcription Bivalent/Poised TSS Strong transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
4	esv1829662	chr22:30171725-30304390	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
5	esv1829425	chr22:30184378-30297376	Genic enhancers Flanking Active TSS Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs13058224	LGALS8	trans	lymphoblastoid	RTeQTL

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:30245000-30250200	Weak transcription	Primary monocytes fromperipheralblood	blood
2	chr22:30245000-30250400	Weak transcription	Monocytes-CD14+_RO01746	blood
3	chr22:30245000-30250600	Weak transcription	Adipose Nuclei	Adipose
4	chr22:30245000-30251400	Weak transcription	Skeletal Muscle Male	skeletal muscle
5	chr22:30245600-30250200	Weak transcription	Primary neutrophils fromperipheralblood	blood

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