Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:32397666..32400035-chr11:32435330..32437389,2	K562	blood:
2	chr11:32431798..32437144-chr11:32439795..32446613,10	K562	blood:

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

rs_ID	r²[population]
rs10767933	0.80[ASN][1000 genomes]
rs10835893	0.80[ASN][1000 genomes]
rs10835904	0.84[ASN][1000 genomes]
rs11824258	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12290546	0.84[ASN][1000 genomes]
rs1799937	0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2234587	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2295081	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2295082	0.86[AFR][1000 genomes];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs3818055	0.83[ASN][1000 genomes]
rs3858445	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs5030201	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs5030207	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs5030218	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs5030317	0.81[ASN][1000 genomes]
rs5030320	0.81[ASN][1000 genomes]
rs6484574	0.80[ASN][1000 genomes]
rs6484575	0.80[ASN][1000 genomes]
rs6484576	0.80[ASN][1000 genomes]
rs6484577	0.84[ASN][1000 genomes]
rs7107082	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 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	nsv1038188	chr11:32410305-32449799	Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
3	nsv1044547	chr11:32435753-32465233	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:32433400-32437200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
2	chr11:32434000-32442400	Weak transcription	Right Ventricle	heart
3	chr11:32434200-32438000	Weak transcription	Ovary	ovary
4	chr11:32435400-32437800	Weak transcription	K562	blood
5	chr11:32435600-32438000	Weak transcription	Fetal Kidney	kidney
6	chr11:32436400-32441800	Enhancers	Dnd41	blood

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