| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:30156268-30156394 | Rare:33 | ||||
| chr8:30744138-30744220 | Common:1; Rare:42 | ||||
| chr8:32548008-32548241 | Rare:62 | ||||
| chr8:33484683-33484755 | Rare:20 | ||||
| chr8:33485022-33485219 | Common:2; Rare:68 | ||||
| chr8:37736393-37736763 | Common:3; Rare:126 | ||||
| chr8:37762384-37762723 | Common:2; Rare:123 | ||||
| chr8:37849830-37849963 | Common:1; Rare:52 | ||||
| chr8:38105224-38105626 | Common:3; Rare:130 | ||||
| chr8:38105779-38105929 | Rare:46 | ||||
| chr8:38106135-38106403 | Common:1; Rare:64 | ||||
| chr8:38176430-38176605 | Common:1; Rare:56 | ||||
| chr8:38176674-38177049 | Common:5; Rare:119 | ||||
| chr8:38269120-38269248 | Rare:51 | ||||
| chr8:38468024-38468203 | Common:1; Rare:49; Clinvar (benign):2 |