| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:12377061-12377740 | Common:14; Rare:335; Clinvar:2; Clinvar (benign):16 | ||||
| chr18:12419660-12420076 | Common:7; Rare:123 | ||||
| chr18:12657880-12658258 | Common:13; Rare:283 | ||||
| chr18:12702594-12703094 | Common:8; Rare:383 | ||||
| chr18:12883730-12883998 | Common:6; Rare:157 | ||||
| chr18:12884156-12884389 | Common:2; Rare:118 | ||||
| chr18:12947666-12948098 | Common:6; Rare:230 | ||||
| chr18:12948219-12948545 | Common:2; Rare:209 | ||||
| chr18:12991137-12991427 | Common:4; Rare:197 | ||||
| chr18:13217040-13217460 | Common:1; Rare:114 | ||||
| chr18:13217385-13217834 | Common:4; Rare:122 | ||||
| chr18:13541950-13542530 | Common:7; Rare:164 | ||||
| chr18:13726408-13726732 | Common:8; Rare:231 | ||||
| chr18:21110790-21111320 | Rare:184 | ||||
| chr18:21111434-21111826 | Common:1; Rare:101 |