| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:13726482-13726726 | Common:3; Rare:92 | ||||
| chr18:21111541-21111947 | Common:2; Rare:124 | ||||
| chr18:21612241-21612418 | Common:1; Rare:61 | ||||
| chr18:21704738-21704932 | Rare:60 | ||||
| chr18:22169362-22169589 | Common:1; Rare:58 | ||||
| chr18:22933204-22933561 | Common:5; Rare:114; Clinvar:7; Clinvar (benign):3 | ||||
| chr18:22933776-22933923 | Common:1; Rare:57 | ||||
| chr18:23453044-23453325 | Rare:91 | ||||
| chr18:23529812-23529883 | Common:1; Rare:12 | ||||
| chr18:23586381-23586532 | Common:2; Rare:68; Clinvar:3; Clinvar (benign):1 | ||||
| chr18:23689296-23689619 | Rare:71 | ||||
| chr18:26090513-26090685 | Common:1; Rare:77 | ||||
| chr18:26657384-26657508 | Rare:32 | ||||
| chr18:28177006-28177428 | Common:3; Rare:202 | ||||
| chr18:31498057-31498259 | Common:1; Rare:64; Clinvar:4; Clinvar (benign):5 |