| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:97764465-97764608 | Rare:30 | ||||
| chr3:98522844-98523073 | Common:1; Rare:73 | ||||
| chr3:98593530-98593774 | Common:3; Rare:97; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:98732248-98732369 | Rare:24 | ||||
| chr3:98732371-98732603 | Rare:38 | ||||
| chr3:98732605-98732832 | Rare:51 | ||||
| chr3:98733177-98733473 | Common:2; Rare:75 | ||||
| chr3:98733689-98733896 | Common:1; Rare:46 | ||||
| chr3:98782933-98783148 | Common:6; Rare:38 | ||||
| chr3:98783733-98784014 | Common:1; Rare:40 | ||||
| chr3:98784911-98784990 | Common:2; Rare:23 | ||||
| chr3:98801182-98801622 | Common:2; Rare:91 | ||||
| chr3:98900693-98900944 | Rare:48 | ||||
| chr3:98900957-98901080 | Rare:37 | ||||
| chr3:98901098-98901171 | Common:1; Rare:27 |