Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:15881637..15884616-chr11:15884653..15886949,2	K562	blood:

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10766286	0.84[ASN][1000 genomes]
rs10832527	0.88[AFR][1000 genomes];0.84[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs10832528	0.81[AMR][1000 genomes]
rs11023740	0.83[ASN][1000 genomes]
rs11023745	0.84[ASN][1000 genomes]
rs11023749	0.83[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs11023751	0.82[AFR][1000 genomes];0.81[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs11023754	0.81[AFR][1000 genomes];0.84[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs11023756	0.84[AMR][1000 genomes]
rs11604993	0.89[AFR][1000 genomes];0.84[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs12576777	0.84[ASN][1000 genomes]
rs1371909	0.83[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs1440702	0.81[AMR][1000 genomes]
rs1440718	0.90[ASN][1000 genomes]
rs1440719	0.82[AFR][1000 genomes];0.84[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs1440720	0.85[AFR][1000 genomes];0.84[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs1866819	0.83[AMR][1000 genomes]
rs1866821	0.90[ASN][1000 genomes]
rs2011772	0.88[ASN][1000 genomes]
rs2083526	0.82[AFR][1000 genomes];0.84[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs2196961	0.84[AMR][1000 genomes]
rs2218205	0.84[ASN][1000 genomes]
rs2351392	0.84[ASN][1000 genomes]
rs4459259	0.83[ASN][1000 genomes]
rs4757377	0.81[AMR][1000 genomes]
rs55842281	0.83[ASN][1000 genomes]
rs56183020	0.81[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs61878488	0.80[ASN][1000 genomes]
rs727324	0.82[ASN][1000 genomes]
rs874189	0.88[ASN][1000 genomes]
rs882148	0.86[AFR][1000 genomes];0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832073	chr11:15822409-15984078	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:15873400-15882800	Weak transcription	Right Atrium	heart
2	chr11:15877200-15885200	Weak transcription	Cortex derived primary cultured neurospheres	brain
3	chr11:15880600-15885000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr11:15881200-15886600	Enhancers	Fetal Heart	heart

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