| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:134411859-134412033 | Rare:52 | ||||
| chr5:134648726-134648878 | Rare:41 | ||||
| chr5:136046975-136047357 | Common:2; Rare:90; Clinvar:2; Clinvar (benign):1 | ||||
| chr5:136132777-136132944 | Common:1; Rare:51 | ||||
| chr5:138033010-138033172 | Common:1; Rare:59 | ||||
| chr5:138178920-138179205 | Common:3; Rare:58 | ||||
| chr5:138213302-138213547 | Rare:53 | ||||
| chr5:138331777-138332127 | Common:2; Rare:84 | ||||
| chr5:138543104-138543512 | Common:2; Rare:125 | ||||
| chr5:138575247-138575479 | Common:1; Rare:117 | ||||
| chr5:139561737-139561803 | Rare:27 | ||||
| chr5:140564326-140564468 | Common:1; Rare:42 | ||||
| chr5:140564573-140564856 | Rare:77 | ||||
| chr5:140647588-140647888 | Common:5; Rare:121; Clinvar:4; Clinvar (benign):3 | ||||
| chr5:140691268-140691471 | Common:2; Rare:74; Clinvar:7; Clinvar (benign):1 |