Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:15948178..15950643-chr7:15952055..15954693,2	K562	blood:

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

rs_ID	r²[population]
rs10244390	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10262767	0.87[ASN][1000 genomes]
rs10486787	1.00[ASN][1000 genomes]
rs1072965	0.82[EUR][1000 genomes]
rs12155069	0.87[ASN][1000 genomes]
rs1406098	0.80[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs17457220	0.87[ASN][1000 genomes]
rs1942643	0.86[ASN][1000 genomes]
rs2052028	0.87[ASN][1000 genomes]
rs2389572	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs36076917	1.00[ASN][1000 genomes]
rs59125965	0.82[EUR][1000 genomes]
rs6966591	1.00[ASN][1000 genomes]
rs6968544	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73060245	0.86[ASN][1000 genomes]
rs73060294	0.87[ASN][1000 genomes]
rs73060296	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73062182	1.00[ASN][1000 genomes]
rs73062188	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7793631	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7798899	1.00[ASN][1000 genomes]
rs7799669	1.00[ASN][1000 genomes]
rs9654940	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9654941	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9690090	0.87[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	nsv523199	chr7:15582208-16042596	Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
2	nsv1016642	chr7:15884061-16799788	Genic enhancers Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
3	nsv1017958	chr7:15910153-15956470	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:15946400-15955400	Weak transcription	Rectal Smooth Muscle	rectum

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