| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:2571969-2572040 | Rare:10 | ||||
| chr18:2655103-2655252 | Common:1; Rare:54 | ||||
| chr18:2655335-2655461 | Rare:28 | ||||
| chr18:2655469-2655792 | Common:5; Rare:130 | ||||
| chr18:2655804-2655994 | Common:1; Rare:60 | ||||
| chr18:2656030-2656131 | Common:3; Rare:45; Clinvar:4; Clinvar (benign):1 | ||||
| chr18:2846673-2847097 | Common:3; Rare:101 | ||||
| chr18:2906052-2906284 | Common:1; Rare:77 | ||||
| chr18:2906676-2907082 | Common:5; Rare:147 | ||||
| chr18:3012805-3012926 | Common:1; Rare:36 | ||||
| chr18:3013205-3013315 | Common:3; Rare:46 | ||||
| chr18:3247225-3247666 | Common:5; Rare:123 | ||||
| chr18:3247689-3247971 | Rare:89 | ||||
| chr18:3248089-3248305 | Common:5; Rare:47 | ||||
| chr18:3261216-3261459 | Rare:35 |