| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:58573500-58573587 | Common:1; Rare:21 | ||||
| chr2:263999-264117 | Common:1; Rare:41 | ||||
| chr2:264558-264975 | Common:4; Rare:153 | ||||
| chr2:677364-677557 | Common:1; Rare:80 | ||||
| chr2:1744457-1744579 | Common:1; Rare:46 | ||||
| chr2:3379649-3379814 | Common:2; Rare:69 | ||||
| chr2:3519452-3519582 | Common:2; Rare:48 | ||||
| chr2:3558269-3558545 | Common:6; Rare:103 | ||||
| chr2:3575107-3575345 | Common:2; Rare:69; Clinvar:2; Clinvar (benign):5 | ||||
| chr2:9423145-9423731 | Common:1; Rare:160 | ||||
| chr2:9474498-9474630 | Common:6; Rare:62 | ||||
| chr2:9555637-9556029 | Common:2; Rare:131 | ||||
| chr2:9630313-9630837 | Common:6; Rare:216 | ||||
| chr2:9630950-9631316 | Common:3; Rare:118 | ||||
| chr2:10302731-10302925 | Common:2; Rare:68 |