| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:124546856-124547025 | Rare:40 | ||||
| chr8:124549871-124550143 | Common:1; Rare:56; Clinvar (benign):1 | ||||
| chr8:124673330-124673669 | Common:2; Rare:66 | ||||
| chr8:124728106-124728246 | Common:1; Rare:21 | ||||
| chr8:124728376-124728767 | Common:5; Rare:118 | ||||
| chr8:124998211-124998610 | Common:4; Rare:157 | ||||
| chr8:125091709-125091938 | Common:2; Rare:80; Clinvar (benign):3 | ||||
| chr8:125430206-125430414 | Common:1; Rare:45 | ||||
| chr8:125431748-125431772 | Rare:3 | ||||
| chr8:125432704-125432870 | Common:1; Rare:18 | ||||
| chr8:126558362-126558638 | Common:1; Rare:105 | ||||
| chr8:127735220-127735617 | Common:1; Rare:70 | ||||
| chr8:127735862-127736092 | Rare:52 | ||||
| chr8:127736118-127736329 | Common:3; Rare:52 | ||||
| chr8:131904046-131904184 | Rare:57 |