| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:140647588-140647924 | Common:5; Rare:137; Clinvar:4; Clinvar (benign):3 | ||||
| chr5:140664778-140664909 | Common:2; Rare:34 | ||||
| chr5:140691309-140691497 | Common:1; Rare:69; Clinvar:7 | ||||
| chr5:140800761-140801123 | Common:4; Rare:47 | ||||
| chr5:140821602-140821654 | Common:1; Rare:9 | ||||
| chr5:140834002-140834269 | Common:2; Rare:47 | ||||
| chr5:141172537-141172704 | Common:1; Rare:32 | ||||
| chr5:141320722-141320928 | Common:3; Rare:71 | ||||
| chr5:141417611-141417741 | Common:1; Rare:35 | ||||
| chr5:141475837-141476016 | Rare:37 | ||||
| chr5:141484649-141485185 | Common:2; Rare:113 | ||||
| chr5:141636821-141636997 | Common:1; Rare:72 | ||||
| chr5:141682191-141682328 | Common:1; Rare:45 | ||||
| chr5:141923721-141923904 | Common:1; Rare:52 | ||||
| chr5:142108470-142109008 | Common:5; Rare:158 |