| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:145835344-145835525 | Common:2; Rare:44 | ||||
| chr5:146182492-146182853 | Common:3; Rare:98 | ||||
| chr5:148383729-148384036 | Rare:83 | ||||
| chr5:149141400-149141834 | Common:1; Rare:107 | ||||
| chr5:149345393-149345534 | Common:1; Rare:46 | ||||
| chr5:149551282-149551631 | Common:1; Rare:77 | ||||
| chr5:150449683-150449797 | Common:4; Rare:42 | ||||
| chr5:150624549-150624891 | Rare:90 | ||||
| chr5:150640504-150640793 | Rare:53 | ||||
| chr5:150700960-150701156 | Common:2; Rare:81 | ||||
| chr5:151025056-151025491 | Common:2; Rare:97 | ||||
| chr5:151080935-151081183 | Common:1; Rare:80 | ||||
| chr5:151157688-151157891 | Common:1; Rare:50 | ||||
| chr5:154038876-154039010 | Common:1; Rare:48 | ||||
| chr5:154477613-154477848 | Common:1; Rare:85; Clinvar:1; Clinvar (benign):2 |