Variant report

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10053101	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10079491	0.94[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10476518	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1157899	0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11956893	0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs13355597	1.00[ASN][1000 genomes]
rs13360184	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1460748	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6875613	0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6875617	0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6891846	1.00[ASN][1000 genomes]
rs73131381	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73131385	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73131390	0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73131401	1.00[ASN][1000 genomes]
rs73133207	1.00[ASN][1000 genomes]
rs73133209	1.00[ASN][1000 genomes]
rs9314083	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9314084	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9688292	1.00[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	nsv830400	chr5:92515026-92738896	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv830401	chr5:92518294-92703611	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:92672600-92684400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr5:92677000-92685400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr5:92678800-92684200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr5:92679000-92684000	Weak transcription	HSMM	muscle
5	chr5:92683600-92684200	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr5:92683600-92684200	Bivalent Enhancer	HepG2	liver
7	chr5:92683600-92684800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr5:92683600-92684800	Enhancers	Fetal Muscle Trunk	muscle
9	chr5:92683600-92685600	Enhancers	Muscle Satellite Cultured Cells	--
10	chr5:92683800-92684000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr5:92683800-92685000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr5:92683800-92686400	Enhancers	HMEC	breast

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