| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:140303057-140303160 | Common:1; Rare:34 | ||||
| chr5:140346597-140346721 | Common:1; Rare:34 | ||||
| chr5:140564518-140564858 | Rare:85 | ||||
| chr5:140647585-140647915 | Common:5; Rare:136; Clinvar:4; Clinvar (benign):3 | ||||
| chr5:140691313-140691646 | Common:1; Rare:116; Clinvar:9; Clinvar (benign):1 | ||||
| chr5:141636810-141637001 | Common:2; Rare:83 | ||||
| chr5:141682195-141682407 | Common:2; Rare:57 | ||||
| chr5:141923613-141923877 | Common:1; Rare:69 | ||||
| chr5:142324984-142325236 | Rare:82 | ||||
| chr5:142644237-142644438 | Common:1; Rare:36 | ||||
| chr5:143404422-143404611 | Common:2; Rare:43 | ||||
| chr5:144170572-144170874 | Common:2; Rare:99 | ||||
| chr5:146182489-146182861 | Common:3; Rare:105 | ||||
| chr5:146203411-146203649 | Common:2; Rare:72 | ||||
| chr5:148383740-148384022 | Rare:76 |