| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:53591445-53591613 | Common:1; Rare:34 | ||||
| chr4:54064410-54064538 | Rare:33 | ||||
| chr4:54064548-54064862 | Common:5; Rare:106 | ||||
| chr4:54277313-54277490 | Common:1; Rare:39; Clinvar:9; Clinvar (benign):4 | ||||
| chr4:55125299-55125329 | Rare:7 | ||||
| chr4:55346171-55346376 | Common:3; Rare:67; Clinvar:3; Clinvar (benign):2 | ||||
| chr4:55395776-55395987 | Common:3; Rare:70; Clinvar:2 | ||||
| chr4:55398134-55398474 | Common:3; Rare:60 | ||||
| chr4:55398667-55398876 | Common:2; Rare:24 | ||||
| chr4:55546602-55547020 | Common:6; Rare:128 | ||||
| chr4:55948720-55948848 | Rare:25 | ||||
| chr4:56387423-56387528 | Rare:35 | ||||
| chr4:56435464-56435973 | Common:6; Rare:167 | ||||
| chr4:56436037-56436314 | Rare:103 | ||||
| chr4:56467461-56467699 | Common:2; Rare:94; Clinvar (benign):5 |