| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:104985560-104985829 | Common:4; Rare:98 | ||||
| chr14:105021003-105021440 | Common:1; Rare:159 | ||||
| chr14:105248438-105248639 | Common:4; Rare:98 | ||||
| chr14:105300897-105301117 | Rare:60 | ||||
| chr14:105419719-105420057 | Common:1; Rare:102 | ||||
| chr15:22786584-22786783 | Rare:83; Clinvar:2; Clinvar (benign):2 | ||||
| chr15:22838481-22838839 | Common:2; Rare:127 | ||||
| chr15:23039440-23039695 | Common:1; Rare:116 | ||||
| chr15:25438463-25438558 | Rare:29; Clinvar (benign):1 | ||||
| chr15:25438977-25439237 | Common:3; Rare:102 | ||||
| chr15:28886104-28886206 | Common:1; Rare:32 | ||||
| chr15:29269745-29269980 | Common:2; Rare:104 | ||||
| chr15:29822005-29822153 | Rare:54 | ||||
| chr15:29822155-29822280 | Rare:43 | ||||
| chr15:29822362-29822498 | Rare:64 |