Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:59385467..59387589-chr8:59391157..59392732,2	K562	blood:

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

rs_ID	r²[population]
rs10107182	0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1030431	0.87[CEU][hapmap]
rs10504255	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11996829	0.87[CEU][hapmap]
rs13263105	0.87[CEU][hapmap]
rs13277801	0.91[CEU][hapmap];0.84[EUR][1000 genomes]
rs1580180	0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1993453	0.87[CEU][hapmap];0.84[EUR][1000 genomes]
rs2016886	0.87[CEU][hapmap]
rs2081687	0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2326077	0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4738679	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4738680	0.85[EUR][1000 genomes]
rs4738684	0.87[AFR][1000 genomes];0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4738685	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs6471717	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6982486	0.87[CEU][hapmap]
rs6985620	0.85[EUR][1000 genomes]
rs7005978	0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7007181	0.91[CEU][hapmap]
rs7018333	0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7826120	0.85[EUR][1000 genomes]
rs8192870	0.90[CEU][hapmap];0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs983812	0.92[EUR][1000 genomes];0.95[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	nsv890938	chr8:59355053-59809785	Enhancers Strong transcription Flanking Active TSS Weak transcription Genic enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:59391200-59395000	Enhancers	Liver	Liver
2	chr8:59391400-59392400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
3	chr8:59391400-59392400	Weak transcription	Pancreas	Pancrea
4	chr8:59391600-59392400	Weak transcription	Right Atrium	heart
5	chr8:59391800-59393800	Enhancers	HepG2	liver

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