Variant report

Variant	rs2736270
Chromosome Location	chr8:11192593-11192594
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:11190703..11193064-chr8:11198301..11200688,2	K562	blood:

Extended variants
information (count: 84 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:74)

rs_ID	r²[population]
rs10096194	0.83[CEU][hapmap]
rs10110557	0.83[CEU][hapmap]
rs1047950	0.95[CEU][hapmap];0.83[YRI][hapmap];0.84[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10503421	0.83[CEU][hapmap]
rs11250130	0.90[CEU][hapmap];0.81[EUR][1000 genomes]
rs11777746	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11781637	0.90[CEU][hapmap];0.81[EUR][1000 genomes]
rs11782430	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs11784572	0.86[YRI][hapmap];0.87[ASN][1000 genomes]
rs12547100	0.82[AMR][1000 genomes]
rs12550129	0.82[AMR][1000 genomes]
rs12676062	0.80[ASN][1000 genomes]
rs12676613	0.80[ASN][1000 genomes]
rs12681987	0.91[CEU][hapmap];0.95[YRI][hapmap]
rs13260727	0.86[CEU][hapmap];0.82[AMR][1000 genomes]
rs13268126	0.82[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs13274106	0.82[AMR][1000 genomes]
rs1435277	0.95[CEU][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17741537	0.82[CEU][hapmap]
rs17797894	0.87[CEU][hapmap]
rs1865521	0.81[AMR][1000 genomes]
rs2043508	0.80[EUR][1000 genomes]
rs2060456	0.82[CEU][hapmap]
rs2060459	0.82[CEU][hapmap]
rs2246606	0.95[CEU][hapmap];0.90[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2249804	0.90[CEU][hapmap];0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2250028	0.90[CEU][hapmap];0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2251473	0.80[AFR][1000 genomes];0.83[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs2293859	0.82[CEU][hapmap]
rs2293860	0.82[CEU][hapmap]
rs2409756	0.86[CEU][hapmap]
rs2572371	0.91[CEU][hapmap]
rs2572382	0.95[CEU][hapmap];0.96[YRI][hapmap];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2572385	0.95[CEU][hapmap];0.95[YRI][hapmap];0.83[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2572386	0.86[CEU][hapmap]
rs2572387	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2572397	0.84[YRI][hapmap];0.81[AFR][1000 genomes];0.83[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs2572398	0.91[YRI][hapmap];0.83[AMR][1000 genomes]
rs2572404	0.93[AFR][1000 genomes];0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2572452	0.91[CEU][hapmap]
rs2736264	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2736265	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2736266	0.82[EUR][1000 genomes]
rs2736273	0.98[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2736278	0.90[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2736280	0.81[CEU][hapmap]
rs2736282	0.86[CEU][hapmap]
rs2736283	0.86[CEU][hapmap]
rs2736288	0.86[CEU][hapmap];0.80[EUR][1000 genomes]
rs2736290	0.85[CEU][hapmap]
rs2736292	0.86[CEU][hapmap]
rs2736295	0.86[CEU][hapmap]
rs2736298	0.81[AMR][1000 genomes]
rs34389419	0.84[AMR][1000 genomes]
rs34482136	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs34964435	0.82[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs35009431	0.82[AMR][1000 genomes]
rs35418978	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3779891	0.82[CEU][hapmap]
rs4363158	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4413734	0.82[CEU][hapmap]
rs4448232	0.81[AMR][1000 genomes]
rs5029571	0.82[CEU][hapmap]
rs6601582	0.91[CEU][hapmap];0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6601584	0.82[AMR][1000 genomes]
rs6601585	0.86[CEU][hapmap]
rs7005469	0.81[CEU][hapmap]
rs7816606	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7819395	0.83[CEU][hapmap]
rs7828263	0.84[AMR][1000 genomes]
rs7832747	0.87[YRI][hapmap]
rs7838897	0.83[CEU][hapmap]
rs7839053	0.83[CEU][hapmap]
rs7839307	0.96[AFR][1000 genomes];0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 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

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs2736270	C8orf5	Cis_1M	lymphoblastoid	RTeQTL
rs2736270	MTMR9	Cis_1M	lymphoblastoid	RTeQTL

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:11182400-11193600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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