Variant report

(count:4 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	TEAD4	chr8:125928349-125929087	K562	blood:	n/a	n/a
2	TAL1	chr8:125928427-125929012	K562	blood:	n/a	n/a
3	UBTF	chr8:125928949-125928991	K562	blood:	n/a	n/a
4	GATA1	chr8:125928125-125929342	PBDE	blood:	n/a	n/a

No data

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

No.	Distal block	Cell Line	Cell type
1	chr8:125922613..125924246-chr8:125927138..125929372,2	MCF-7	breast:
2	chr8:125928560..125931491-chr8:125949569..125951872,2	MCF-7	breast:
3	chr8:125869478..125872586-chr8:125926416..125930050,3	MCF-7	breast:
4	chr1:117602865..117605635-chr8:125927109..125929309,2	MCF-7	breast:
5	chr8:125903181..125907429-chr8:125925929..125929993,4	K562	blood:
6	chr8:125928235..125930330-chr8:125931694..125933573,2	K562	blood:
7	chr8:125928423..125931250-chr8:125983352..125985484,3	MCF-7	breast:
8	chr8:125928235..125930086-chr8:125931694..125934034,2	K562	blood:
9	chr8:125927702..125929777-chr8:125936123..125937814,2	MCF-7	breast:

No data

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10956221	0.83[AMR][1000 genomes]
rs11987831	0.87[AMR][1000 genomes]
rs12681718	0.85[AMR][1000 genomes]
rs13252227	0.89[AMR][1000 genomes]
rs28810782	0.82[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs4871561	0.85[AMR][1000 genomes]
rs4871566	0.87[AMR][1000 genomes]
rs6470295	0.87[AMR][1000 genomes]
rs6470297	0.87[AMR][1000 genomes]
rs6470299	0.87[AMR][1000 genomes]
rs6470301	0.87[AMR][1000 genomes]
rs6470304	0.83[AMR][1000 genomes]
rs6470310	0.82[AMR][1000 genomes]
rs6470312	0.82[AMR][1000 genomes]
rs7011950	0.82[AMR][1000 genomes]
rs7016723	0.87[AMR][1000 genomes]
rs7387254	0.82[AMR][1000 genomes]
rs7388465	0.82[AMR][1000 genomes]
rs7461228	0.89[AMR][1000 genomes]
rs7463183	0.87[AMR][1000 genomes]
rs7463584	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7464601	0.89[AMR][1000 genomes]
rs7464910	0.83[AMR][1000 genomes]
rs7813655	0.84[AFR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7820918	0.83[AMR][1000 genomes]
rs7833872	0.86[AFR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7845589	0.87[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv891434	chr8:125630655-126324432	Strong transcription Enhancers Weak transcription Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
2	nsv1030803	chr8:125868684-125969635	Weak transcription Enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
3	nsv1024405	chr8:125868684-125971035	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
4	nsv1020502	chr8:125868684-125972572	Active TSS Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:125925600-125931200	Weak transcription	Monocytes-CD14+_RO01746	blood
2	chr8:125926200-125929600	Weak transcription	HepG2	liver
3	chr8:125928200-125929800	Enhancers	K562	blood

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