| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:4657542-4657736 | Common:3; Rare:40 | ||||
| chr12:5741091-5741253 | Rare:24 | ||||
| chr12:5881804-5881909 | Rare:16 | ||||
| chr12:6200217-6200410 | Common:2; Rare:55 | ||||
| chr12:6363337-6363472 | Common:2; Rare:51; Clinvar (benign):1 | ||||
| chr12:6363788-6363847 | Common:1; Rare:17 | ||||
| chr12:6375432-6375496 | Rare:7 | ||||
| chr12:6451809-6452062 | Common:3; Rare:45 | ||||
| chr12:6452079-6452155 | Common:1; Rare:19 | ||||
| chr12:6470599-6470839 | Common:1; Rare:84 | ||||
| chr12:6493088-6493399 | Common:7; Rare:91 | ||||
| chr12:6493778-6494154 | Common:2; Rare:113 | ||||
| chr12:6534252-6534914 | Common:9; Rare:269 | ||||
| chr12:6535140-6535440 | Common:4; Rare:94 | ||||
| chr12:6568234-6568388 | Rare:59 |