| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:140401427-140401678 | Common:2; Rare:48 | ||||
| chr5:140547412-140547682 | Common:3; Rare:51 | ||||
| chr5:140557404-140557515 | Rare:68 | ||||
| chr5:140564326-140564449 | Common:1; Rare:39 | ||||
| chr5:140564550-140564841 | Rare:76 | ||||
| chr5:140639286-140639496 | Common:3; Rare:56 | ||||
| chr5:140647579-140647896 | Common:5; Rare:129; Clinvar:4; Clinvar (benign):3 | ||||
| chr5:140691300-140691633 | Common:1; Rare:120; Clinvar:10; Clinvar (benign):1 | ||||
| chr5:140794534-140794867 | Rare:59 | ||||
| chr5:140807003-140807088 | Common:1; Rare:13 | ||||
| chr5:140856427-140856603 | Rare:65 | ||||
| chr5:140926220-140926335 | Rare:41 | ||||
| chr5:141320725-141320928 | Common:3; Rare:71 | ||||
| chr5:141636808-141636964 | Common:2; Rare:70 | ||||
| chr5:141682195-141682328 | Common:1; Rare:43 |