Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:32465131..32467084-chr11:32469130..32471983,4	K562	blood:
2	chr11:32468457..32470421-chr11:32472103..32475103,3	K562	blood:

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs10742278	0.80[ASN][1000 genomes]
rs10767936	0.82[ASN][1000 genomes]
rs10767937	0.80[ASN][1000 genomes]
rs10767938	0.82[ASN][1000 genomes]
rs10835913	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10835914	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10835915	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11031787	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11031788	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11031790	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12575247	0.82[AMR][1000 genomes]
rs1799925	0.81[AMR][1000 genomes]
rs2073187	0.82[ASN][1000 genomes]
rs2418912	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2900753	0.82[EUR][1000 genomes]
rs34163689	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs3858451	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs3858453	0.80[ASN][1000 genomes]
rs3858457	0.82[ASN][1000 genomes]
rs59518979	0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs61889255	0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs61889256	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7103128	0.82[ASN][1000 genomes]
rs7115829	0.82[ASN][1000 genomes]
rs975665	0.82[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	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:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:32468600-32469400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr11:32468800-32469200	Enhancers	Fetal Kidney	kidney
3	chr11:32468800-32469600	Enhancers	Dnd41	blood
4	chr11:32468800-32471400	Enhancers	K562	blood
5	chr11:32469000-32469200	Enhancers	Primary hematopoietic stem cells short term culture	blood
6	chr11:32469000-32487800	Weak transcription	Ovary	ovary

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