Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:149596030..149597712-chr6:149600814..149603008,2	K562	blood:

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs1001965	0.82[ASN][1000 genomes]
rs1446561	0.83[ASN][1000 genomes]
rs1446562	0.83[ASN][1000 genomes]
rs2011315	0.81[ASN][1000 genomes]
rs4609053	0.82[ASN][1000 genomes]
rs4897102	0.82[ASN][1000 genomes]
rs4897103	0.82[ASN][1000 genomes]
rs4897104	0.82[ASN][1000 genomes]
rs4897105	0.82[ASN][1000 genomes]
rs4897106	0.82[ASN][1000 genomes]
rs4897110	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6570957	0.82[ASN][1000 genomes]
rs6570961	0.82[ASN][1000 genomes]
rs6570962	0.83[ASN][1000 genomes]
rs6903389	0.83[ASN][1000 genomes]
rs6904464	0.83[ASN][1000 genomes]
rs6906793	0.82[ASN][1000 genomes]
rs6907145	0.82[ASN][1000 genomes]
rs6907747	0.82[ASN][1000 genomes]
rs6908247	0.82[ASN][1000 genomes]
rs6908296	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6912297	0.83[ASN][1000 genomes]
rs6912567	0.83[ASN][1000 genomes]
rs6912622	0.83[ASN][1000 genomes]
rs6921428	0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6928940	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6929714	0.82[ASN][1000 genomes]
rs6938137	0.81[ASN][1000 genomes]
rs7756413	0.82[ASN][1000 genomes]
rs9285518	0.83[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs9322171	0.83[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs9390669	0.82[ASN][1000 genomes]
rs9404024	0.86[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs9404025	0.85[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs999120	0.83[AMR][1000 genomes];0.97[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1024776	chr6:149398652-149654593	Weak transcription Active TSS Bivalent Enhancer Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:149599600-149602000	Enhancers	Primary monocytes fromperipheralblood	blood

Quick Search: