Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:108936870..108939701-chr11:108941192..108943026,2	K562	blood:

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs1509714	0.86[EUR][1000 genomes]
rs2010140	1.00[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs72996777	1.00[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs72996779	0.86[EUR][1000 genomes]
rs72998751	1.00[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs72998759	1.00[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs72998765	1.00[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs72998771	1.00[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs72998773	1.00[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs72998783	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs72998789	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs73000660	1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs73000662	1.00[AFR][1000 genomes]
rs73000680	1.00[AFR][1000 genomes]
rs73000682	1.00[AFR][1000 genomes]
rs73000688	1.00[AFR][1000 genomes]
rs73000691	1.00[AFR][1000 genomes]
rs73000695	1.00[AFR][1000 genomes]
rs73002606	1.00[AFR][1000 genomes]
rs73002610	1.00[AFR][1000 genomes]
rs73002677	1.00[AFR][1000 genomes]
rs73002679	1.00[AFR][1000 genomes]
rs73002681	1.00[AFR][1000 genomes]
rs73002683	1.00[AFR][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	nsv1040650	chr11:108859584-109174553	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv898390	chr11:108893765-109003536	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	esv1815918	chr11:108900487-108948487	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv481	chr11:108921271-108946545	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:108941400-108943400	Enhancers	Fetal Heart	heart
2	chr11:108941600-108943400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr11:108941600-108943400	Enhancers	HMEC	breast
4	chr11:108941800-108943200	Enhancers	Skeletal Muscle Male	skeletal muscle
5	chr11:108941800-108943200	Enhancers	Skeletal Muscle Female	skeletal muscle
6	chr11:108942000-108942600	Weak transcription	Left Ventricle	heart
7	chr11:108942000-108943400	Enhancers	Fetal Brain Male	brain
8	chr11:108942000-108946800	Weak transcription	Psoas Muscle	Psoas

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