Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:134225992-134226407 | Common:1; Rare:136 | ||||
chr5:134226631-134226728 | Common:1; Rare:14 | ||||
chr5:134371031-134371184 | Common:1; Rare:39 | ||||
chr5:134411855-134412008 | Rare:49 | ||||
chr5:134648726-134648835 | Rare:26 | ||||
chr5:135399128-135399343 | Rare:57 | ||||
chr5:135578934-135579200 | Common:2; Rare:77 | ||||
chr5:136133650-136133911 | Common:2; Rare:52 | ||||
chr5:138033052-138033170 | Common:1; Rare:41 | ||||
chr5:138178598-138178724 | Rare:33 | ||||
chr5:138543060-138543518 | Common:3; Rare:135 | ||||
chr5:138575247-138575291 | Rare:15 | ||||
chr5:138753271-138753507 | Common:2; Rare:80 | ||||
chr5:139198277-139198531 | Rare:83; Clinvar (benign):1 | ||||
chr5:139561728-139561782 | Rare:27 |