Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:15971634..15973484-chr5:15977480..15979036,2	K562	blood:

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

rs_ID	r²[population]
rs10051749	0.81[ASN][1000 genomes]
rs10076986	0.82[ASN][1000 genomes]
rs11133826	0.82[ASN][1000 genomes]
rs12655516	0.83[ASN][1000 genomes]
rs1393266	0.81[AFR][1000 genomes]
rs1502027	0.86[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs168747	0.83[ASN][1000 genomes]
rs181833	0.92[ASN][1000 genomes]
rs250488	0.85[AFR][1000 genomes]
rs250490	0.85[ASN][1000 genomes]
rs250496	0.92[ASN][1000 genomes]
rs250497	0.92[ASN][1000 genomes]
rs250498	0.80[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs250500	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs250501	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs250503	0.83[ASN][1000 genomes]
rs250504	0.83[ASN][1000 genomes]
rs250505	0.81[ASN][1000 genomes]
rs2599492	0.84[ASN][1000 genomes]
rs2599503	0.83[ASN][1000 genomes]
rs32823	0.84[ASN][1000 genomes]
rs32824	0.88[ASN][1000 genomes]
rs32825	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs32826	0.83[ASN][1000 genomes]
rs32827	0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs32828	0.82[ASN][1000 genomes]
rs32829	0.83[ASN][1000 genomes]
rs32830	0.83[ASN][1000 genomes]
rs4701645	0.81[ASN][1000 genomes]
rs4701646	0.81[ASN][1000 genomes]
rs4702120	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	nsv830216	chr5:15860662-16060420	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region miRNA	4 gene(s)	inside rSNPs	diseases
2	nsv427712	chr5:15883439-16055856	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region miRNA	4 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	chr5:15970400-15981000	Weak transcription	Right Ventricle	heart

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