Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr17:38582887..38585427-chr17:38586447..38588752,2	K562	blood:
2	chr17:38580560..38584947-chr17:38585760..38591436,7	K562	blood:

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

rs_ID	r²[population]
rs11078945	0.89[YRI][hapmap]
rs11867902	0.85[YRI][hapmap]
rs11871146	0.89[YRI][hapmap]
rs1530363	0.88[CEU][hapmap];0.81[CHB][hapmap];1.00[GIH][hapmap];0.80[JPT][hapmap];0.88[MKK][hapmap];0.93[TSI][hapmap];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs16965783	0.95[CHB][hapmap];1.00[CHD][hapmap];0.98[GIH][hapmap];0.94[JPT][hapmap];0.96[TSI][hapmap];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2586112	0.80[CHD][hapmap];0.98[GIH][hapmap];0.84[JPT][hapmap];0.89[TSI][hapmap];0.90[EUR][1000 genomes]
rs2715556	0.88[ASW][hapmap];0.98[GIH][hapmap];0.84[JPT][hapmap];0.93[TSI][hapmap];0.85[YRI][hapmap]
rs2715557	0.88[EUR][1000 genomes]
rs471692	0.80[CHD][hapmap];0.98[GIH][hapmap];0.84[JPT][hapmap];0.89[TSI][hapmap];0.82[EUR][1000 genomes]
rs473198	0.81[CHB][hapmap];1.00[GIH][hapmap];0.80[JPT][hapmap];0.93[TSI][hapmap];0.94[EUR][1000 genomes]
rs474510	0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs495511	0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs506728	0.83[JPT][hapmap]
rs507564	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs525217	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs525812	0.88[CEU][hapmap];0.84[CHB][hapmap];0.81[JPT][hapmap];0.95[EUR][1000 genomes]
rs552857	0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs557498	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs558068	0.85[EUR][1000 genomes]
rs62066565	0.90[EUR][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	nsv833445	chr17:38466474-38637969	Flanking Active TSS Enhancers Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
2	nsv908223	chr17:38530799-38609187	Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	24 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:38575400-38588600	Weak transcription	Fetal Stomach	stomach
2	chr17:38579600-38598800	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr17:38582600-38587800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr17:38582800-38588000	Weak transcription	Spleen	Spleen
5	chr17:38583000-38588200	Weak transcription	K562	blood
6	chr17:38583600-38589600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
7	chr17:38584000-38592600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
8	chr17:38584400-38589200	Weak transcription	Fetal Thymus	thymus
9	chr17:38584600-38600200	Weak transcription	Primary T helper naive cells from peripheral blood	blood

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