| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:141878224-141878467 | Common:3; Rare:116 | ||||
| chr5:141878474-141878634 | Common:2; Rare:41 | ||||
| chr5:141923701-141923956 | Common:2; Rare:145 | ||||
| chr5:141923940-141924260 | Common:5; Rare:92 | ||||
| chr5:141958760-141959090 | Common:2; Rare:88 | ||||
| chr5:141968841-141969282 | Common:6; Rare:216 | ||||
| chr5:142012834-142013172 | Common:3; Rare:132 | ||||
| chr5:142108685-142108897 | Common:4; Rare:125 | ||||
| chr5:142324920-142325210 | Rare:172 | ||||
| chr5:142770160-142770472 | Common:1; Rare:102 | ||||
| chr5:142874665-142874894 | Common:1; Rare:48 | ||||
| chr5:143400521-143401162 | Common:8; Rare:295; Clinvar:4; Clinvar (benign):2 | ||||
| chr5:143402969-143403167 | Common:2; Rare:78 | ||||
| chr5:143403568-143403970 | Common:1; Rare:254 | ||||
| chr5:143404218-143404622 | Common:3; Rare:142 |