| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:144413552-144413723 | Common:1; Rare:51; Clinvar:1 | ||||
| chr8:144428484-144428726 | Common:3; Rare:92 | ||||
| chr8:144477880-144478057 | Common:4; Rare:70 | ||||
| chr8:144755408-144755614 | Rare:89 | ||||
| chr8:144787279-144787419 | Common:2; Rare:49 | ||||
| chr8:144792318-144792562 | Common:3; Rare:92 | ||||
| chr8:144798802-144798919 | Common:1; Rare:32 | ||||
| chr8:144827253-144827592 | Common:1; Rare:87 | ||||
| chr8:144852982-144853113 | Rare:50 | ||||
| chr8:144901408-144901729 | Common:1; Rare:91 | ||||
| chr8:144950814-144950920 | Common:2; Rare:37 | ||||
| chr8:145052198-145052494 | Common:10; Rare:82 | ||||
| chr9:214697-214868 | Common:4; Rare:95; Clinvar (benign):1 | ||||
| chr9:215041-215215 | Common:5; Rare:104; Clinvar (benign):1 | ||||
| chr9:707021-707221 | Common:4; Rare:68 |