Variant report

Variant	rs11032654
Chromosome Location	chr11:34423774-34423775
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:34417375..34420835-chr11:34422366..34425189,3	K562	blood:
2	chr11:34417920..34420835-chr11:34423610..34425189,2	K562	blood:
3	chr11:34408037..34410021-chr11:34421049..34423975,2	K562	blood:
4	chr11:34422105..34424628-chr11:34424992..34426893,2	K562	blood:

Variant related genes	Relation type
ENSG00000220204	Chromatin interaction

Extended variants
information (count: 55 )
Associated
traits (count: 8 )

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

rs_ID	r²[population]
rs1001179	1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[MEX][hapmap];1.00[YRI][hapmap]
rs1008491	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs10836215	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10836223	0.80[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10836230	0.88[CEU][hapmap];0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10836234	0.88[CEU][hapmap];0.91[GIH][hapmap];1.00[MEX][hapmap];0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11032661	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11032667	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11032669	1.00[CEU][hapmap];0.85[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11032670	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11032671	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11032695	0.88[CEU][hapmap];0.94[GIH][hapmap];1.00[MEX][hapmap];0.87[TSI][hapmap];0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11032719	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs11032722	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs11032723	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs11032724	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs11604331	0.88[CEU][hapmap];1.00[CHB][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.81[MKK][hapmap];0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12361866	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1267468	1.00[YRI][hapmap]
rs12790004	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12790378	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12793666	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12797274	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12797675	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12804506	1.00[CEU][hapmap];0.87[CHD][hapmap];0.94[GIH][hapmap];0.94[MEX][hapmap];1.00[TSI][hapmap];0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12804689	1.00[CEU][hapmap];0.94[GIH][hapmap];0.94[MEX][hapmap];1.00[TSI][hapmap];0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12806377	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12807961	0.88[CEU][hapmap];0.91[GIH][hapmap];1.00[MEX][hapmap];0.82[TSI][hapmap];0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12808450	0.88[CEU][hapmap];0.91[GIH][hapmap];1.00[MEX][hapmap];0.82[TSI][hapmap];0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs17269931	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs17352313	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2231825	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[MKK][hapmap]
rs2231828	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[MKK][hapmap];1.00[YRI][hapmap]
rs2476504	1.00[JPT][hapmap]
rs34329347	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs34533645	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs35725681	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4756135	1.00[YRI][hapmap]
rs494024	1.00[CHB][hapmap];0.83[GIH][hapmap];1.00[JPT][hapmap];0.97[MKK][hapmap];1.00[YRI][hapmap]
rs499406	1.00[CHB][hapmap];0.83[GIH][hapmap];1.00[JPT][hapmap];0.97[MKK][hapmap];1.00[YRI][hapmap]
rs511895	1.00[CHB][hapmap];0.83[GIH][hapmap];1.00[JPT][hapmap];0.85[MKK][hapmap]
rs524167	1.00[CHB][hapmap];0.83[GIH][hapmap];1.00[JPT][hapmap];0.83[MKK][hapmap]
rs533425	1.00[CHB][hapmap];0.83[GIH][hapmap];1.00[JPT][hapmap];0.97[MKK][hapmap];1.00[YRI][hapmap]
rs55892947	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs560807	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs59090359	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs61880810	1.00[ASN][1000 genomes]
rs66679411	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs873466	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs910089	0.86[AMR][1000 genomes];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	nsv897205	chr11:34248229-34507213	Enhancers Weak transcription Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
2	nsv897207	chr11:34253683-34621004	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
3	nsv897208	chr11:34257064-34562247	Strong transcription Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
4	nsv897209	chr11:34309519-34548906	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
5	nsv983151	chr11:34401342-34444667	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Active TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

mRNA abundance (count:8)

SNP	Gene	Cis/trans	Tissue	Source
rs11032654	TEX264	trans	parietal	SCAN
rs11032654	ABTB2	cis	Whole Blood	GTEx
rs11032654	DEPDC7	cis	parietal	SCAN
rs11032654	CAT	cis	lymphoblastoid	seeQTL
rs11032654	CAT	cis	Whole Blood	GTEx
rs11032654	CAT	Cis_1M	lymphoblastoid	RTeQTL
rs11032654	CAT	cis	multi-tissue	Pritchard
rs11032654	CAT	cis	parietal	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:34419000-34428600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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