Variant report

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10765617	0.88[EUR][1000 genomes]
rs10831063	0.94[EUR][1000 genomes]
rs10831064	0.94[EUR][1000 genomes]
rs10831076	0.88[EUR][1000 genomes]
rs10831077	0.88[EUR][1000 genomes]
rs10831079	0.89[EUR][1000 genomes]
rs11020426	0.94[EUR][1000 genomes]
rs11020427	0.94[EUR][1000 genomes]
rs11020450	0.89[EUR][1000 genomes]
rs11020452	0.89[EUR][1000 genomes]
rs11020453	0.89[EUR][1000 genomes]
rs11020454	0.88[EUR][1000 genomes]
rs11020455	0.87[EUR][1000 genomes]
rs11606802	0.91[EUR][1000 genomes]
rs12222957	0.91[EUR][1000 genomes]
rs12802772	0.93[ASN][1000 genomes]
rs1939561	0.93[ASN][1000 genomes]
rs1939570	0.89[EUR][1000 genomes]
rs1939571	0.89[EUR][1000 genomes]
rs1939572	0.89[EUR][1000 genomes]
rs1954783	0.91[EUR][1000 genomes]
rs2155247	0.89[EUR][1000 genomes]
rs34679231	0.95[EUR][1000 genomes]
rs4121453	0.91[ASN][1000 genomes]
rs4237559	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4753089	0.94[EUR][1000 genomes]
rs4753093	0.91[EUR][1000 genomes]
rs4753094	0.89[EUR][1000 genomes]
rs4753480	0.93[EUR][1000 genomes]
rs67011570	0.87[EUR][1000 genomes]
rs7119935	0.99[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7120590	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs948017	0.89[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv898181	chr11:93072843-93662459	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	119 gene(s)	inside rSNPs	diseases
2	nsv1039623	chr11:93141461-93328739	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:93317400-93320200	Weak transcription	K562	blood
2	chr11:93318800-93319600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr11:93319200-93319600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
4	chr11:93319200-93323200	Enhancers	Stomach Mucosa	stomach
5	chr11:93319400-93320400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr11:93319400-93320400	Weak transcription	Gastric	stomach
7	chr11:93319400-93320800	Weak transcription	Pancreas	Pancrea
8	chr11:93319400-93324400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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