Variant report

Variant	rs4445713
Chromosome Location	chr12:8619364-8619365
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 98 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:86)

rs_ID	r²[population]
rs10734709	0.81[AMR][1000 genomes]
rs10734713	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10743393	0.84[AMR][1000 genomes]
rs10743396	0.84[AMR][1000 genomes]
rs10770722	0.81[AMR][1000 genomes]
rs10770723	0.81[AMR][1000 genomes]
rs10770734	0.84[AMR][1000 genomes]
rs10770735	0.84[AMR][1000 genomes]
rs10770736	0.84[AMR][1000 genomes]
rs10770737	0.84[AMR][1000 genomes]
rs10770738	0.84[AMR][1000 genomes]
rs10770739	0.84[AMR][1000 genomes]
rs10770740	0.81[AMR][1000 genomes]
rs10770775	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10770776	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10770793	0.80[AMR][1000 genomes]
rs11045643	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11045652	0.93[EUR][1000 genomes]
rs11045708	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11045757	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11045810	0.81[AMR][1000 genomes]
rs12300621	0.81[AMR][1000 genomes]
rs12302015	0.84[AMR][1000 genomes]
rs12302854	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12304190	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12308954	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12322968	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12423976	0.93[EUR][1000 genomes]
rs4242888	0.81[AMR][1000 genomes]
rs4242889	0.90[AFR][1000 genomes];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4242891	0.90[AFR][1000 genomes];0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4242892	0.90[AFR][1000 genomes];0.87[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4242893	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4242895	0.93[EUR][1000 genomes]
rs4255605	0.84[AMR][1000 genomes]
rs4258429	0.93[EUR][1000 genomes]
rs4264222	0.82[AMR][1000 genomes]
rs4268555	0.82[AMR][1000 genomes]
rs4303299	0.98[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4334073	0.87[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4343097	0.81[AMR][1000 genomes]
rs4388969	0.84[AMR][1000 genomes]
rs4402377	0.84[AMR][1000 genomes]
rs4427631	0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4435079	0.81[AMR][1000 genomes]
rs4447245	0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4457803	0.93[EUR][1000 genomes]
rs4460883	0.89[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4477485	0.81[AMR][1000 genomes]
rs4528410	0.81[AMR][1000 genomes]
rs4565980	0.83[AMR][1000 genomes]
rs4622339	0.81[AMR][1000 genomes]
rs4623977	0.84[AMR][1000 genomes]
rs4623978	0.81[AMR][1000 genomes]
rs4628756	0.84[AMR][1000 genomes]
rs4638374	0.81[AMR][1000 genomes]
rs4640002	0.84[AMR][1000 genomes]
rs4641551	0.81[AMR][1000 genomes]
rs4882942	0.81[AMR][1000 genomes]
rs4882949	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4882950	0.85[AMR][1000 genomes]
rs4882951	0.82[AMR][1000 genomes]
rs4883148	0.82[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs4883149	0.89[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs4883154	0.81[AFR][1000 genomes];0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4883164	0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6487136	0.81[AMR][1000 genomes]
rs7132871	0.81[AMR][1000 genomes]
rs7134303	0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7302011	0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7309596	0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7312686	0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7312713	0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7315590	0.89[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7315873	0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7962791	0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7963053	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7964875	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7968198	0.81[AMR][1000 genomes]
rs7969317	0.81[AMR][1000 genomes]
rs7969325	0.81[AMR][1000 genomes]
rs7976692	0.93[EUR][1000 genomes]
rs7976958	0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7977465	0.82[EUR][1000 genomes]
rs7978179	0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7978218	0.93[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2758292	chr12:7856819-8623987	Enhancers Active TSS Genic enhancers Flanking Active TSS Weak transcription 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	93 gene(s)	inside rSNPs	diseases
2	esv2759877	chr12:7856819-8623987	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	93 gene(s)	inside rSNPs	diseases
3	nsv428270	chr12:7856819-8623987	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	93 gene(s)	inside rSNPs	diseases
4	nsv1040302	chr12:8245364-8695612	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
5	nsv541397	chr12:8245364-8695612	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
6	nsv427902	chr12:8276546-8623987	Active TSS Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
7	nsv1044543	chr12:8449100-8792569	Flanking Active TSS Weak transcription ZNF genes & repeats Enhancers Bivalent/Poised TSS Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
8	nsv1039504	chr12:8494944-8780137	Enhancers Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
9	nsv557342	chr12:8599397-8774527	Enhancers Flanking Active TSS Genic enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
10	nsv933050	chr12:8602789-8775989	Enhancers Genic enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
11	nsv518772	chr12:8615809-8667579	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
12	nsv518125	chr12:8615809-8671274	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs4445713	CLEC6A	cis	Whole Blood	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:8617200-8620200	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr12:8618400-8619400	Active TSS	Monocytes-CD14+_RO01746	blood
3	chr12:8619200-8620400	Enhancers	Primary neutrophils fromperipheralblood	blood

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