Variant report

Variant	rs11032851
Chromosome Location	chr11:34785980-34785981
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 63 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:57)

rs_ID	r²[population]
rs10466455	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10501135	0.84[EUR][1000 genomes]
rs10742325	0.84[EUR][1000 genomes]
rs10742326	0.84[EUR][1000 genomes]
rs10768093	0.86[EUR][1000 genomes]
rs10768094	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10768097	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10768099	0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10768100	0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10836295	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10836300	0.84[ASN][1000 genomes]
rs10836302	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10836303	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10836304	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10836306	0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10836307	0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10836310	0.84[EUR][1000 genomes]
rs10836311	0.84[EUR][1000 genomes]
rs10836312	0.84[EUR][1000 genomes]
rs11032839	0.83[EUR][1000 genomes]
rs11032840	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11032848	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11032849	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11032852	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11032860	0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11032866	0.84[EUR][1000 genomes]
rs11032868	0.83[EUR][1000 genomes]
rs11032870	0.84[EUR][1000 genomes]
rs11032872	0.84[EUR][1000 genomes]
rs1113588	0.83[ASN][1000 genomes]
rs11499809	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12280698	0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12286940	0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1396885	0.84[EUR][1000 genomes]
rs1396887	0.81[ASN][1000 genomes]
rs1396888	0.84[ASN][1000 genomes]
rs1396889	0.84[ASN][1000 genomes]
rs1472975	0.81[EUR][1000 genomes]
rs1509666	0.84[ASN][1000 genomes]
rs1509667	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1509668	0.84[ASN][1000 genomes]
rs1588354	0.84[EUR][1000 genomes]
rs1588355	0.81[ASN][1000 genomes]
rs1605880	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2136508	0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2136509	0.81[ASN][1000 genomes]
rs2421740	0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs3980643	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7112043	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7116210	0.81[ASN][1000 genomes]
rs7122506	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7124685	0.84[ASN][1000 genomes]
rs7124826	0.84[ASN][1000 genomes]
rs7933927	0.81[ASN][1000 genomes]
rs7942593	0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7942701	0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs906902	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832117	chr11:34639008-34831199	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
2	nsv1051492	chr11:34641598-34789331	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
3	nsv1052008	chr11:34641598-34794024	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
4	nsv869812	chr11:34648088-34810956	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
5	nsv832118	chr11:34743123-34903951	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv897214	chr11:34764251-34821948	Weak transcription Bivalent Enhancer Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	n/a

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs11032851	APIP	cis	lung	GTEx
rs11032851	APIP	cis	Skin Sun Exposed Lower leg	GTEx

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:34760400-34787000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr11:34765200-34787000	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr11:34775000-34786400	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr11:34779400-34787000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr11:34780200-34790800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr11:34780600-34790800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr11:34780600-34792400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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