| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:104815954-104816232 | Common:2; Rare:181 | ||||
| chr14:105496250-105496600 | Common:7; Rare:143 | ||||
| chr14:106844624-106845024 | Common:7; Rare:146 | ||||
| chr14:106845370-106845920 | Common:9; Rare:200 | ||||
| chr15:22494700-22494926 | Rare:67 | ||||
| chr15:22665010-22665470 | Common:4; Rare:196 | ||||
| chr15:22939180-22939801 | Common:13; Rare:230 | ||||
| chr15:25375350-25376101 | Common:2; Rare:245; Clinvar:10; Clinvar (benign):12; Clinvar (pathogenic):2 | ||||
| chr15:28832052-28832401 | Common:4; Rare:97 | ||||
| chr15:31157570-31158040 | Common:10; Rare:162 | ||||
| chr15:38073180-38073601 | Common:3; Rare:137 | ||||
| chr15:40081600-40082030 | Common:2; Rare:162 | ||||
| chr15:40098780-40099200 | Common:2; Rare:146 | ||||
| chr15:40323463-40323703 | Common:3; Rare:74 | ||||
| chr15:40582780-40583130 | Rare:144 |