| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:2656226-2656345 | Common:1; Rare:37; Clinvar:1; Clinvar (benign):1 | ||||
| chr18:2846672-2846794 | Common:2; Rare:38 | ||||
| chr18:2846953-2847124 | Rare:41 | ||||
| chr18:2905703-2905954 | Common:9; Rare:77 | ||||
| chr18:2906058-2906412 | Common:1; Rare:116 | ||||
| chr18:2906615-2906829 | Common:2; Rare:71 | ||||
| chr18:2906908-2907063 | Common:2; Rare:61 | ||||
| chr18:3012803-3013022 | Common:1; Rare:66 | ||||
| chr18:3013045-3013459 | Common:3; Rare:152 | ||||
| chr18:3246788-3247110 | Common:1; Rare:64 | ||||
| chr18:3247163-3247673 | Common:6; Rare:139 | ||||
| chr18:3247704-3247913 | Rare:68 | ||||
| chr18:3248019-3248035 | |||||
| chr18:3248155-3248267 | Common:4; Rare:27 | ||||
| chr18:3261448-3261645 | Common:2; Rare:53 |