Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:32460248..32463699-chr11:32486018..32490383,4	K562	blood:

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs10219425	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10835911	0.87[EUR][1000 genomes]
rs10835916	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10835917	0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11031791	0.87[EUR][1000 genomes]
rs11031792	0.87[EUR][1000 genomes]
rs11031793	0.87[EUR][1000 genomes]
rs11031796	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2418931	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs3858454	0.88[EUR][1000 genomes]
rs3858455	0.88[EUR][1000 genomes]
rs3858456	0.88[EUR][1000 genomes]
rs3858459	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs3858461	0.81[ASN][1000 genomes]
rs3930317	0.88[EUR][1000 genomes]
rs4275604	0.86[EUR][1000 genomes]
rs4304749	0.87[EUR][1000 genomes]
rs4980793	0.86[EUR][1000 genomes]
rs7103000	0.86[EUR][1000 genomes]
rs7126322	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7395210	0.88[EUR][1000 genomes]
rs7944133	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7948813	0.88[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	nsv832108	chr11:32395937-32560583	Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	esv2753303	chr11:32447324-32494924	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:32487800-32490600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr11:32488200-32490200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
3	chr11:32488400-32490000	Weak transcription	Dnd41	blood
4	chr11:32488400-32499200	Weak transcription	K562	blood
5	chr11:32489600-32491400	Enhancers	Primary monocytes fromperipheralblood	blood

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