| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:100951252-100951553 | Common:3; Rare:110 | ||||
| chr8:102864159-102864299 | Rare:60 | ||||
| chr8:103298720-103298939 | Common:1; Rare:53 | ||||
| chr8:103372188-103372550 | Rare:66 | ||||
| chr8:103415056-103415455 | Common:6; Rare:209 | ||||
| chr8:109334072-109334405 | Common:1; Rare:84 | ||||
| chr8:119832826-119832877 | Common:1; Rare:18 | ||||
| chr8:120445102-120445238 | Common:1; Rare:30 | ||||
| chr8:123396206-123396508 | Common:1; Rare:146 | ||||
| chr8:124474535-124474763 | Rare:83 | ||||
| chr8:124474963-124475105 | Rare:46 | ||||
| chr8:124539044-124539255 | Common:2; Rare:104; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr8:124998273-124998557 | Common:1; Rare:109 | ||||
| chr8:127735884-127736081 | Rare:44 | ||||
| chr8:141391889-141392053 | Common:1; Rare:57 |