| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:75261598-75261910 | Common:4; Rare:91; Clinvar (benign):1 | ||||
| chr17:75393740-75394031 | Common:1; Rare:68 | ||||
| chr17:75667185-75667370 | Common:4; Rare:57 | ||||
| chr17:75979118-75979271 | Rare:40; Clinvar:4 | ||||
| chr17:76103735-76103867 | Common:4; Rare:37 | ||||
| chr17:76726531-76726865 | Common:5; Rare:116 | ||||
| chr17:81666580-81666759 | Common:1; Rare:73 | ||||
| chr17:81683721-81684021 | Common:4; Rare:147 | ||||
| chr18:3247380-3247622 | Common:1; Rare:64 | ||||
| chr18:9136693-9136814 | Rare:43 | ||||
| chr18:12702678-12703083 | Common:3; Rare:165 | ||||
| chr18:12947719-12948092 | Common:2; Rare:97 | ||||
| chr18:35290237-35290341 | Common:1; Rare:34 | ||||
| chr18:36828772-36829124 | Common:1; Rare:127 | ||||
| chr18:45967261-45967546 | Common:1; Rare:103 |