Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:81479552..81481692-chr14:81684705..81687037,3	K562	blood:
2	chr14:81476596..81478510-chr14:81478665..81481342,2	K562	blood:

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10483973	0.97[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11847353	0.83[AFR][1000 genomes];0.82[AMR][1000 genomes]
rs11847606	0.86[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs11851225	0.89[AFR][1000 genomes];0.88[AMR][1000 genomes]
rs13379243	0.83[AMR][1000 genomes]
rs13379251	0.83[AMR][1000 genomes]
rs17111397	1.00[ASN][1000 genomes]
rs2371465	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28410258	0.87[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs28410717	0.85[AFR][1000 genomes];0.88[AMR][1000 genomes]
rs28750114	0.83[AMR][1000 genomes]
rs34331892	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4403990	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4617779	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6574619	0.94[AMR][1000 genomes]
rs6574620	0.94[AMR][1000 genomes]
rs7152004	0.94[AMR][1000 genomes]
rs7152497	0.86[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs7154960	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7161100	1.00[MEX][hapmap]
rs73349940	0.83[AMR][1000 genomes]
rs73349970	0.81[AFR][1000 genomes];0.88[AMR][1000 genomes]
rs8007755	0.83[AMR][1000 genomes]
rs8008523	0.83[AMR][1000 genomes]
rs8012937	0.83[AMR][1000 genomes]
rs8013119	0.83[AMR][1000 genomes]
rs8023193	0.88[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][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	nsv869348	chr14:80921098-81535754	Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv1052999	chr14:81468860-81599074	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
3	nsv542144	chr14:81468860-81599074	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:81455800-81492200	Weak transcription	Fetal Thymus	thymus
2	chr14:81468000-81486600	Weak transcription	Thymus	Thymus
3	chr14:81478000-81482600	Weak transcription	Dnd41	blood

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