Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:2468888-2469167 | Common:3; Rare:106 | ||||
chr4:4248169-4248261 | Common:3; Rare:45 | ||||
chr4:4290110-4290274 | Common:3; Rare:66 | ||||
chr4:4541939-4542143 | Common:1; Rare:82 | ||||
chr4:7068028-7068373 | Common:5; Rare:118 | ||||
chr4:7939814-7940050 | Common:2; Rare:98 | ||||
chr4:8440702-8441017 | Rare:124 | ||||
chr4:15655295-15655477 | Common:1; Rare:82 | ||||
chr4:15681458-15681869 | Common:3; Rare:142 | ||||
chr4:16898610-16898980 | Common:14; Rare:59 | ||||
chr4:17614551-17614649 | Common:2; Rare:42 | ||||
chr4:17810687-17811072 | Common:4; Rare:121 | ||||
chr4:24584473-24584702 | Common:1; Rare:76 | ||||
chr4:25160411-25160732 | Common:3; Rare:90; Clinvar:2; Clinvar (benign):1 | ||||
chr4:25376979-25377302 | Common:3; Rare:99 |