| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:94062877-94063069 | Rare:52 | ||||
| chr3:97764454-97764824 | Common:1; Rare:87; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:97821890-97822216 | Common:2; Rare:111 | ||||
| chr3:97961557-97961634 | Common:1; Rare:22 | ||||
| chr3:98732422-98732551 | Rare:21 | ||||
| chr3:98732619-98732963 | Rare:85 | ||||
| chr3:98733129-98733471 | Common:3; Rare:83 | ||||
| chr3:99817568-99817934 | Rare:111 | ||||
| chr3:99876072-99876400 | Common:2; Rare:92 | ||||
| chr3:100260798-100261066 | Rare:82 | ||||
| chr3:100261313-100261357 | Rare:7 | ||||
| chr3:100492233-100492663 | Common:2; Rare:122 | ||||
| chr3:100709249-100709613 | Common:5; Rare:121; Clinvar (benign):1 | ||||
| chr3:101513110-101513365 | Common:8; Rare:65 | ||||
| chr3:101574056-101574279 | Common:1; Rare:78 |