| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:3261757-3261930 | Common:3; Rare:46 | ||||
| chr18:3261954-3262243 | Common:3; Rare:99 | ||||
| chr18:3262245-3262459 | Common:8; Rare:53 | ||||
| chr18:3262695-3262718 | Rare:5 | ||||
| chr18:3447508-3447706 | Rare:49 | ||||
| chr18:3447929-3448569 | Common:7; Rare:167 | ||||
| chr18:3448929-3449428 | Common:7; Rare:110 | ||||
| chr18:3449434-3449769 | Common:2; Rare:84 | ||||
| chr18:3449927-3450552 | Common:2; Rare:192; Clinvar (benign):2 | ||||
| chr18:3451444-3451772 | Common:4; Rare:98 | ||||
| chr18:3453754-3453775 | Rare:3 | ||||
| chr18:3453781-3453791 | Rare:2 | ||||
| chr18:3454055-3454159 | Rare:21 | ||||
| chr18:3454797-3454833 | Rare:11 | ||||
| chr18:5294523-5294671 | Rare:48 |