| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:102864159-102864299 | Rare:60 | ||||
| chr8:103415071-103415476 | Common:6; Rare:211 | ||||
| chr8:108248683-108248872 | Rare:75 | ||||
| chr8:109334060-109334459 | Common:1; Rare:106 | ||||
| chr8:116755771-116755913 | Common:1; Rare:72 | ||||
| chr8:116766372-116766586 | Common:1; Rare:54 | ||||
| chr8:119832826-119832934 | Common:1; Rare:40 | ||||
| chr8:120445075-120445421 | Common:1; Rare:85 | ||||
| chr8:121641377-121641502 | Rare:22 | ||||
| chr8:123041991-123042360 | Common:1; Rare:115 | ||||
| chr8:123274228-123274321 | Rare:13 | ||||
| chr8:123416388-123416831 | Rare:113 | ||||
| chr8:124474549-124474788 | Rare:87 | ||||
| chr8:124538981-124539283 | Common:2; Rare:156; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr8:125091712-125091916 | Common:2; Rare:70; Clinvar (benign):3 |