Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:8216194..8218883-chr11:8223154..8225386,2	K562	blood:
2	chr11:8214526..8217689-chr11:8218013..8220798,3	K562	blood:

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs11041793	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11041794	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11041795	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11041796	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11041799	0.82[AFR][1000 genomes];0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11041803	0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11041804	0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12786434	0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs17227568	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs3849993	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs3861071	0.85[ASN][1000 genomes]
rs3911309	0.82[AFR][1000 genomes];0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs3911310	0.82[AFR][1000 genomes];0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4412746	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4539318	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4564325	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4636658	0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs55885664	0.83[EUR][1000 genomes]
rs56090029	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs67639141	0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7114892	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.88[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	nsv896981	chr11:8152080-8227964	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv1054339	chr11:8153582-8263173	Bivalent Enhancer Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:8214600-8218400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr11:8214600-8218400	Weak transcription	Brain Substantia Nigra	brain
3	chr11:8214800-8218000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr11:8215200-8217200	Weak transcription	Brain Hippocampus Middle	brain
5	chr11:8215400-8218400	Weak transcription	Primary B cells from peripheral blood	blood
6	chr11:8215400-8220200	Enhancers	Primary monocytes fromperipheralblood	blood
7	chr11:8215800-8220200	Enhancers	Monocytes-CD14+_RO01746	blood
8	chr11:8216800-8217200	Enhancers	Brain Cingulate Gyrus	brain
9	chr11:8216800-8217600	Enhancers	Brain Inferior Temporal Lobe	brain

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