| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:97821890-97822074 | Rare:66 | ||||
| chr3:98901638-98902008 | Common:1; Rare:140 | ||||
| chr3:99817560-99817995 | Rare:134 | ||||
| chr3:100260767-100261045 | Rare:76 | ||||
| chr3:100400758-100400932 | Common:1; Rare:49 | ||||
| chr3:100401398-100401576 | Common:1; Rare:33 | ||||
| chr3:100492420-100492642 | Common:2; Rare:72 | ||||
| chr3:100709218-100709451 | Common:4; Rare:81; Clinvar (benign):1 | ||||
| chr3:101513112-101513310 | Common:8; Rare:41 | ||||
| chr3:101561742-101561971 | Common:2; Rare:84 | ||||
| chr3:101574045-101574276 | Common:1; Rare:81 | ||||
| chr3:101677059-101677166 | Rare:46 | ||||
| chr3:101686493-101686860 | Common:2; Rare:150 | ||||
| chr3:101779092-101779253 | Common:3; Rare:51 | ||||
| chr3:105366437-105366919 | Common:4; Rare:125 |