| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:121736855-121737113 | Common:4; Rare:92 | ||||
| chr2:127885954-127885975 | Rare:3 | ||||
| chr2:128091027-128091358 | Common:8; Rare:109 | ||||
| chr2:130181561-130181700 | Common:1; Rare:45 | ||||
| chr2:130342127-130342242 | Rare:45 | ||||
| chr2:130342642-130342926 | Common:5; Rare:88 | ||||
| chr2:130355754-130356198 | Common:7; Rare:127 | ||||
| chr2:131105211-131105370 | Common:1; Rare:72 | ||||
| chr2:131493038-131493107 | Common:1; Rare:20 | ||||
| chr2:134918601-134918873 | Common:1; Rare:111 | ||||
| chr2:135531209-135531534 | Common:1; Rare:61 | ||||
| chr2:135742631-135742750 | Rare:29 | ||||
| chr2:135985419-135985642 | Common:4; Rare:105; Clinvar (benign):1 | ||||
| chr2:136115921-136116387 | Common:1; Rare:90; Clinvar:1 | ||||
| chr2:136116497-136116523 | Rare:1 |