Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:25758095..25760842-chr10:25796322..25798852,2	K562	blood:

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10047266	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10508700	0.93[ASN][1000 genomes]
rs10741093	0.83[EUR][1000 genomes]
rs1329252	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1536836	0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1536837	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs3923088	0.83[EUR][1000 genomes]
rs4097489	0.81[ASN][1000 genomes]
rs4097490	0.83[ASN][1000 genomes]
rs4747523	0.83[ASN][1000 genomes]
rs4747524	0.86[ASN][1000 genomes]
rs4749038	0.85[ASN][1000 genomes]
rs4749040	0.86[ASN][1000 genomes]
rs5001528	0.82[EUR][1000 genomes]
rs6482488	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7068743	0.85[ASN][1000 genomes]
rs7072700	0.83[ASN][1000 genomes]
rs7082952	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7478285	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs943985	0.87[AFR][1000 genomes];0.84[AMR][1000 genomes];0.93[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	esv3349863	chr10:25614571-25946379	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 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	chr10:25791600-25800400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr10:25792800-25811600	Weak transcription	Cortex derived primary cultured neurospheres	brain

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