Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:140670488..140672458-chr6:140677865..140680641,2	K562	blood:

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs12526285	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12530095	0.90[ASN][1000 genomes]
rs13216392	0.80[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs1390499	0.91[CHB][hapmap];0.86[YRI][hapmap]
rs1832676	0.83[ASN][1000 genomes]
rs1856754	0.90[ASN][1000 genomes]
rs1856756	0.80[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs1856757	0.90[ASN][1000 genomes]
rs201281	0.90[CHB][hapmap]
rs34380839	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs35442760	0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs35927834	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6570390	0.84[ASN][1000 genomes]
rs6570396	0.91[ASN][1000 genomes]
rs669704	0.80[EUR][1000 genomes]
rs675432	0.91[CHB][hapmap]
rs67762923	0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs8180615	0.80[ASN][1000 genomes]
rs9373275	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9376516	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9376517	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9385911	0.91[ASN][1000 genomes]
rs9389788	0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs982369	0.81[CHB][hapmap];0.83[YRI][hapmap]

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	nsv1016532	chr6:140174639-141029988	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	17 gene(s)	inside rSNPs	diseases
2	nsv1015293	chr6:140544956-140798437	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	nsv817390	chr6:140558103-141166039	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:140675200-140683000	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr6:140679000-140683400	Weak transcription	Placenta	Placenta

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