| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:138543095-138543499 | Common:2; Rare:120 | ||||
| chr5:138575300-138575452 | Common:1; Rare:87 | ||||
| chr5:138753231-138753488 | Common:2; Rare:89 | ||||
| chr5:139561733-139561794 | Rare:27 | ||||
| chr5:140303048-140303177 | Common:1; Rare:42 | ||||
| chr5:140557427-140557548 | Common:2; Rare:73 | ||||
| chr5:140647594-140647892 | Common:5; Rare:121; Clinvar:4; Clinvar (benign):3 | ||||
| chr5:140691313-140691653 | Common:1; Rare:121; Clinvar:10; Clinvar (benign):1 | ||||
| chr5:141320742-141320910 | Common:1; Rare:56 | ||||
| chr5:141636809-141636997 | Common:2; Rare:82 | ||||
| chr5:141923726-141923886 | Common:1; Rare:38 | ||||
| chr5:143404449-143404617 | Common:2; Rare:34 | ||||
| chr5:144170585-144170912 | Common:7; Rare:104 | ||||
| chr5:145937640-145937761 | Rare:31 | ||||
| chr5:146182500-146182832 | Common:3; Rare:90 |