| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:96718635-96718664 | Rare:8 | ||||
| chr8:97275323-97275380 | Common:1; Rare:3 | ||||
| chr8:97276669-97276696 | Rare:8 | ||||
| chr8:98630249-98630460 | Rare:37 | ||||
| chr8:99863478-99863777 | Common:1; Rare:57 | ||||
| chr8:100183791-100184052 | Common:3; Rare:46; Clinvar:2 | ||||
| chr8:100184544-100184731 | Common:3; Rare:43; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr8:100316335-100316520 | Common:2; Rare:26 | ||||
| chr8:100347362-100347477 | Rare:14 | ||||
| chr8:101368854-101368916 | Rare:30 | ||||
| chr8:101879572-101879795 | Common:1; Rare:50 | ||||
| chr8:102061019-102061174 | Rare:24 | ||||
| chr8:102062431-102062658 | Common:2; Rare:40 | ||||
| chr8:102485051-102485209 | Rare:42 | ||||
| chr8:102894548-102894738 | Common:1; Rare:34 |