| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:74496747-74496782 | Rare:7 | ||||
| chr18:74499294-74499417 | Common:1; Rare:26 | ||||
| chr18:74499764-74499953 | Common:2; Rare:40 | ||||
| chr18:74597311-74597490 | Common:1; Rare:40 | ||||
| chr18:74597518-74598309 | Common:4; Rare:238 | ||||
| chr18:75208415-75208736 | Common:2; Rare:72 | ||||
| chr18:75209523-75209807 | Common:2; Rare:83 | ||||
| chr18:75210741-75210931 | Common:4; Rare:46; Clinvar:7; Clinvar (benign):1 | ||||
| chr18:76495195-76495613 | Common:2; Rare:100 | ||||
| chr18:76495617-76495712 | Common:2; Rare:28 | ||||
| chr18:76822032-76822563 | Common:12; Rare:145 | ||||
| chr18:76822782-76823012 | Common:3; Rare:86 | ||||
| chr18:77128191-77128437 | Common:3; Rare:45 | ||||
| chr18:77131182-77131604 | Common:2; Rare:98 | ||||
| chr18:77131997-77132224 | Common:2; Rare:69 |