| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:50633677-50633717 | Rare:3 | ||||
| chr5:52988500-52988808 | Common:5; Rare:58 | ||||
| chr5:52995343-52995738 | Common:3; Rare:62 | ||||
| chr5:52998504-52998521 | Rare:3 | ||||
| chr5:53036140-53036469 | Common:4; Rare:53 | ||||
| chr5:53044892-53045186 | Common:2; Rare:70; Clinvar (benign):1 | ||||
| chr5:53051190-53051482 | Common:1; Rare:69; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:53081879-53082073 | Rare:28 | ||||
| chr5:53089782-53090062 | Rare:63; Clinvar (benign):1 | ||||
| chr5:53101475-53101535 | Common:2; Rare:23; Clinvar (benign):1 | ||||
| chr5:53218422-53218448 | Common:1; Rare:3 | ||||
| chr5:53227265-53227415 | Common:3; Rare:39 | ||||
| chr5:53241474-53241510 | Common:3; Rare:7 | ||||
| chr5:53242652-53242707 | Rare:12 | ||||
| chr5:53249652-53249775 | Rare:23 |