Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr9:94282329..94284526-chr9:94349227..94351684,2	K562	blood:
2	chr9:94345770..94347286-chr9:94349788..94351847,2	K562	blood:

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs1027268	0.90[ASN][1000 genomes]
rs1027269	0.90[ASN][1000 genomes]
rs10761121	0.87[ASN][1000 genomes]
rs12551755	0.91[ASN][1000 genomes]
rs1388968	0.90[ASN][1000 genomes]
rs1976220	0.90[ASN][1000 genomes]
rs1976221	0.88[ASN][1000 genomes]
rs2172356	0.90[ASN][1000 genomes]
rs35665194	0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4451437	0.90[ASN][1000 genomes]
rs4744060	0.85[ASN][1000 genomes]
rs4744063	0.80[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4744065	0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4744067	0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4744069	0.90[ASN][1000 genomes]
rs4744071	0.90[ASN][1000 genomes]
rs4744074	0.87[ASN][1000 genomes]
rs4744080	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6479364	0.90[ASN][1000 genomes]
rs7019783	0.90[ASN][1000 genomes]
rs7023804	0.80[ASN][1000 genomes]
rs7026410	0.90[ASN][1000 genomes]
rs7036860	0.85[ASN][1000 genomes]
rs7039512	0.90[ASN][1000 genomes]
rs7041541	0.90[ASN][1000 genomes]
rs7871554	0.89[ASN][1000 genomes]
rs9299393	0.90[ASN][1000 genomes]
rs9409431	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9409611	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3402084	chr9:94349581-94351829	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	esv3482523	chr9:94350525-94352475	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	esv3482524	chr9:94350583-94352422	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	esv3482525	chr9:94350603-94352329	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:94347800-94351200	Weak transcription	Spleen	Spleen
2	chr9:94349200-94351400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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