Variant report

Variant	rs10226883
Chromosome Location	chr7:40889985-40889986
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 50 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs10227436	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10231596	0.89[ASN][1000 genomes]
rs10237052	0.89[ASN][1000 genomes]
rs10263468	0.99[EUR][1000 genomes]
rs10263609	0.81[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10263717	0.81[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1029623	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1029624	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1053953	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1203578	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs17688697	0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17688924	0.98[EUR][1000 genomes]
rs1859845	0.98[EUR][1000 genomes]
rs1921753	0.89[ASN][1000 genomes]
rs1921754	0.89[ASN][1000 genomes]
rs1921755	0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1921756	0.89[ASN][1000 genomes]
rs2005766	0.82[ASN][1000 genomes]
rs2010706	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2108377	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28621645	0.89[ASN][1000 genomes]
rs2876979	0.89[ASN][1000 genomes]
rs4050954	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4050966	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4265100	0.89[ASN][1000 genomes]
rs4425648	0.89[ASN][1000 genomes]
rs4720378	0.89[ASN][1000 genomes]
rs4720379	0.89[ASN][1000 genomes]
rs4720380	0.89[ASN][1000 genomes]
rs4720381	0.89[ASN][1000 genomes]
rs4723982	0.89[ASN][1000 genomes]
rs4723983	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67369140	0.89[ASN][1000 genomes]
rs6952818	0.89[ASN][1000 genomes]
rs6952995	0.89[ASN][1000 genomes]
rs6957123	0.89[ASN][1000 genomes]
rs6963162	0.89[ASN][1000 genomes]
rs6970936	0.89[ASN][1000 genomes]
rs6971120	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs699484	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs732890	0.89[ASN][1000 genomes]
rs758010	0.89[ASN][1000 genomes]
rs7808121	0.89[ASN][1000 genomes]
rs7808304	0.89[ASN][1000 genomes]
rs7808678	0.89[ASN][1000 genomes]
rs7809237	0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7809981	0.86[ASN][1000 genomes]
rs9639838	0.85[ASN][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	nsv1030648	chr7:40218618-41032599	Flanking Active TSS Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv830972	chr7:40814709-40945917	Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:40880200-40905400	Weak transcription	HSMMtube	muscle
2	chr7:40884200-40898800	Weak transcription	NHEK	skin
3	chr7:40884600-40899200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr7:40888400-40890000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr7:40888400-40890200	Enhancers	Osteobl	bone
6	chr7:40889200-40890000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr7:40889400-40890000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr7:40889600-40890000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr7:40889600-40898600	Weak transcription	HMEC	breast

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