| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:139453653-139454185 | Common:5; Rare:149; Clinvar:10; Clinvar (benign):4 | ||||
| chr4:139556186-139556374 | Rare:42 | ||||
| chr4:140373380-140373674 | Common:2; Rare:109 | ||||
| chr4:141220828-141220947 | Rare:35 | ||||
| chr4:143184849-143184958 | Common:5; Rare:41 | ||||
| chr4:143336691-143336903 | Rare:49 | ||||
| chr4:143337085-143337191 | Rare:43 | ||||
| chr4:143391365-143391512 | Common:1; Rare:27 | ||||
| chr4:143513345-143513529 | Common:2; Rare:65 | ||||
| chr4:145098129-145098382 | Rare:82 | ||||
| chr4:145481601-145481703 | Rare:27 | ||||
| chr4:145482455-145482791 | Common:2; Rare:96 | ||||
| chr4:145482958-145483002 | Rare:5 | ||||
| chr4:145525577-145525674 | Rare:15 | ||||
| chr4:145619313-145619406 | Rare:41; Clinvar:2; Clinvar (benign):1 |