Variant report

Variant	rs13253016
Chromosome Location	chr8:11188586-11188587
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 61 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs10096194	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs10098322	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10110557	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11250129	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11774673	0.92[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11781375	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs11782706	0.83[AFR][1000 genomes];0.95[AMR][1000 genomes];0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11784458	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11784544	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11991153	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11994376	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs13248147	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs13250270	0.89[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs13253735	0.92[AMR][1000 genomes];0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs13263127	0.93[AMR][1000 genomes];0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs13266233	0.91[AMR][1000 genomes];0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1435273	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs17797894	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs2293855	0.82[AMR][1000 genomes]
rs2293856	0.85[AMR][1000 genomes]
rs3174048	0.81[AFR][1000 genomes];0.93[AMR][1000 genomes];0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs34237267	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs35631424	0.97[AMR][1000 genomes];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs35747588	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs3779891	0.81[AFR][1000 genomes];0.93[AMR][1000 genomes];0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs58283816	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6601580	0.81[AFR][1000 genomes];0.91[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6988922	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6990563	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6991606	0.83[AMR][1000 genomes]
rs6995404	0.90[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs6996368	0.90[AMR][1000 genomes];0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7005469	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7008205	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7016671	0.81[AFR][1000 genomes];0.91[AMR][1000 genomes];0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7815463	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7815802	0.92[AMR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7815804	0.83[AFR][1000 genomes];0.96[AMR][1000 genomes];0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7816601	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7816636	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7817658	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7819395	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7820895	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7828711	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7831346	0.81[AFR][1000 genomes];0.91[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7833966	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7834139	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7837036	0.81[AMR][1000 genomes]
rs7838897	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7839053	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1035072	chr8:10819444-11480692	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
2	nsv539473	chr8:10819444-11480692	Weak transcription Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
3	nsv529399	chr8:10970091-11805960	Enhancers Strong transcription Weak transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
4	nsv831233	chr8:11046854-11234384	Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
5	nsv1022525	chr8:11066191-11309356	Enhancers Genic enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
6	nsv539474	chr8:11066191-11309356	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
7	nsv1033312	chr8:11126800-11252170	Flanking Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Bivalent Enhancer Enhancers Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
8	esv1821756	chr8:11169178-11217587	Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Active TSS ZNF genes & repeats Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
9	nsv890354	chr8:11176147-11266131	Bivalent Enhancer Strong transcription Weak transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
10	esv34097	chr8:11177372-11489894	Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer 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	17 gene(s)	inside rSNPs	diseases
11	nsv981910	chr8:11185560-11189634	Weak transcription ZNF genes & repeats Strong transcription Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs13253016	C8orf5	Cis_1M	lymphoblastoid	RTeQTL
rs13253016	MTMR9	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:11171600-11191400	Weak transcription	Psoas Muscle	Psoas
2	chr8:11176000-11189000	Weak transcription	Gastric	stomach
3	chr8:11180600-11190200	Weak transcription	A549	lung
4	chr8:11182400-11188800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr8:11182400-11193600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr8:11182600-11188800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
7	chr8:11183000-11188600	Weak transcription	Ovary	ovary
8	chr8:11183000-11189000	Weak transcription	Brain Anterior Caudate	brain
9	chr8:11183000-11189800	Weak transcription	Primary B cells from cord blood	blood
10	chr8:11183800-11190200	Weak transcription	Liver	Liver
11	chr8:11184200-11190200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr8:11187600-11190000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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