| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:138501626-138501997 | Common:6; Rare:245 | ||||
| chr2:142130940-142131075 | Rare:49 | ||||
| chr2:142131380-142131750 | Common:8; Rare:109 | ||||
| chr2:142877464-142877733 | Common:4; Rare:78 | ||||
| chr2:144332441-144332746 | Rare:214 | ||||
| chr2:144517501-144517717 | Common:10; Rare:93 | ||||
| chr2:147844428-147844575 | Common:4; Rare:97 | ||||
| chr2:148020593-148021203 | Common:4; Rare:244; Clinvar (benign):4 | ||||
| chr2:148644595-148644775 | Rare:103 | ||||
| chr2:149330290-149330597 | Common:3; Rare:209 | ||||
| chr2:149586880-149587480 | Common:5; Rare:181; Clinvar:1; Clinvar (benign):5 | ||||
| chr2:149587671-149587863 | Common:2; Rare:90; Clinvar:2 | ||||
| chr2:151261760-151262180 | Common:4; Rare:168 | ||||
| chr2:151289616-151289734 | Common:1; Rare:31 | ||||
| chr2:151289861-151289985 | Rare:35 |