Variant report

Variant	rs7081346
Chromosome Location	chr10:45703753-45703754
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:45696357..45698920-chr10:45703555..45705408,2	K562	blood:

Extended variants
information (count: 60 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:55)

rs_ID	r²[population]
rs10430732	0.97[EUR][1000 genomes]
rs10430733	0.97[EUR][1000 genomes]
rs10458776	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10458777	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs10508892	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs10732899	0.97[EUR][1000 genomes]
rs10751379	0.93[EUR][1000 genomes]
rs10793592	0.97[EUR][1000 genomes]
rs10793593	0.97[EUR][1000 genomes]
rs10793595	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10793596	0.97[EUR][1000 genomes]
rs10793598	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs10793599	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs10793600	0.95[EUR][1000 genomes]
rs10793601	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10793602	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10793603	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10900174	0.95[EUR][1000 genomes]
rs10900175	0.95[EUR][1000 genomes]
rs10900176	0.88[EUR][1000 genomes]
rs10900178	0.97[EUR][1000 genomes]
rs10900179	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10900182	0.98[EUR][1000 genomes]
rs10900183	0.98[EUR][1000 genomes]
rs11239374	0.97[EUR][1000 genomes]
rs11239375	0.97[EUR][1000 genomes]
rs11239387	0.93[EUR][1000 genomes]
rs11239390	0.98[EUR][1000 genomes]
rs12269344	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1856592	0.96[EUR][1000 genomes]
rs2153331	0.97[EUR][1000 genomes]
rs2275847	0.93[EUR][1000 genomes]
rs2282351	0.97[EUR][1000 genomes]
rs2311316	0.95[EUR][1000 genomes]
rs2311317	0.95[EUR][1000 genomes]
rs3851263	0.95[EUR][1000 genomes]
rs4948658	0.97[EUR][1000 genomes]
rs4948953	0.96[EUR][1000 genomes]
rs4948954	0.96[EUR][1000 genomes]
rs4948955	0.97[EUR][1000 genomes]
rs4948959	0.88[EUR][1000 genomes]
rs4948961	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4948962	0.98[EUR][1000 genomes]
rs6593462	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6593463	0.97[EUR][1000 genomes]
rs7074910	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7079140	0.96[EUR][1000 genomes]
rs7081946	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7094007	0.86[EUR][1000 genomes]
rs7898356	0.89[EUR][1000 genomes]
rs7910939	0.94[EUR][1000 genomes]
rs7911066	0.95[EUR][1000 genomes]
rs7917831	0.97[EUR][1000 genomes]
rs7918108	0.97[EUR][1000 genomes]
rs9326532	0.97[EUR][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	esv2750897	chr10:45550145-45820136	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	19 gene(s)	inside rSNPs	diseases
2	nsv895104	chr10:45636867-45715369	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	9 gene(s)	inside rSNPs	diseases
3	nsv895105	chr10:45636867-45928822	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
4	nsv895106	chr10:45659032-45715369	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
5	nsv430166	chr10:45668894-46148794	Bivalent Enhancer Strong transcription Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs7081346	ANUBL1	cis	cerebellum	SCAN
rs7081346	ANUBL1	cis	parietal	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:45701600-45705200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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