| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:3450022-3450397 | Common:1; Rare:102 | ||||
| chr18:3451484-3451688 | Common:2; Rare:79 | ||||
| chr18:3453632-3453854 | Common:5; Rare:51 | ||||
| chr18:3874229-3874377 | Common:2; Rare:43 | ||||
| chr18:3874646-3874764 | Rare:28 | ||||
| chr18:4455225-4455499 | Common:3; Rare:105 | ||||
| chr18:5296898-5297028 | Common:1; Rare:41 | ||||
| chr18:5466284-5466559 | Common:1; Rare:46 | ||||
| chr18:5543973-5544171 | Common:1; Rare:49 | ||||
| chr18:5630639-5630955 | Common:4; Rare:87 | ||||
| chr18:6729858-6729930 | Rare:21 | ||||
| chr18:7117658-7117914 | Common:3; Rare:87 | ||||
| chr18:7946833-7946946 | Rare:26 | ||||
| chr18:9102441-9102796 | Common:2; Rare:150; Clinvar:6; Clinvar (benign):2 | ||||
| chr18:9136552-9137065 | Common:1; Rare:194 |