| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:113584434-113584733 | Rare:87 | ||||
| chr13:113759143-113759232 | Rare:24 | ||||
| chr13:113863940-113864206 | Common:2; Rare:67 | ||||
| chr13:114132500-114132699 | Rare:62 | ||||
| chr13:114281356-114281730 | Common:5; Rare:165 | ||||
| chr13:114281852-114282018 | Common:4; Rare:80 | ||||
| chr14:20343418-20343665 | Common:4; Rare:117 | ||||
| chr14:20413087-20413242 | Common:1; Rare:24 | ||||
| chr14:20454514-20454702 | Rare:59 | ||||
| chr14:20684438-20684619 | Common:2; Rare:30; Clinvar (benign):2 | ||||
| chr14:21070065-21070394 | Common:2; Rare:89 | ||||
| chr14:21211551-21211860 | Common:3; Rare:81 | ||||
| chr14:21476590-21476763 | Rare:78 | ||||
| chr14:21476847-21477271 | Common:2; Rare:141 | ||||
| chr14:21511122-21511560 | Rare:128 |