| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:151409005-151409257 | Common:3; Rare:75 | ||||
| chr4:151409349-151409446 | Rare:19 | ||||
| chr4:152352623-152352882 | Rare:74 | ||||
| chr4:152536056-152536293 | Rare:90 | ||||
| chr4:152779715-152780176 | Common:2; Rare:117 | ||||
| chr4:153344562-153344727 | Common:4; Rare:46 | ||||
| chr4:154550360-154550530 | Rare:52 | ||||
| chr4:156970863-156971279 | Common:1; Rare:76 | ||||
| chr4:156971758-156971945 | Common:1; Rare:70 | ||||
| chr4:158167198-158167328 | Rare:14 | ||||
| chr4:158172354-158172760 | Rare:69 | ||||
| chr4:158172780-158173237 | Common:1; Rare:66 | ||||
| chr4:158210402-158210568 | Common:3; Rare:44 | ||||
| chr4:158671825-158672457 | Common:5; Rare:170; Clinvar:3; Clinvar (benign):2 | ||||
| chr4:158723202-158723447 | Common:2; Rare:106 |