| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:986930-987024 | Rare:22; Clinvar:1 | ||||
| chr4:1113533-1113630 | Common:1; Rare:36 | ||||
| chr4:1172821-1173127 | Common:5; Rare:45 | ||||
| chr4:1249962-1250167 | Common:4; Rare:43 | ||||
| chr4:1289662-1289943 | Common:1; Rare:98 | ||||
| chr4:1720588-1720608 | Rare:6 | ||||
| chr4:1723235-1723545 | Common:4; Rare:88 | ||||
| chr4:2468878-2469167 | Common:4; Rare:108 | ||||
| chr4:2843687-2844022 | Common:3; Rare:121 | ||||
| chr4:2934771-2934931 | Common:4; Rare:74 | ||||
| chr4:2963315-2963571 | Common:2; Rare:97 | ||||
| chr4:3074547-3074692 | Common:2; Rare:43 | ||||
| chr4:3385543-3385703 | Rare:34 | ||||
| chr4:4248179-4248266 | Common:3; Rare:42 | ||||
| chr4:4290102-4290274 | Common:4; Rare:70 |