| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:28386408-28386526 | Common:8; Rare:32 | ||||
| chr8:28490202-28490444 | Common:1; Rare:48 | ||||
| chr8:28494106-28494287 | Common:4; Rare:57 | ||||
| chr8:28889905-28890658 | Rare:207 | ||||
| chr8:29350247-29350329 | Common:1; Rare:30 | ||||
| chr8:29350645-29351006 | Common:2; Rare:90 | ||||
| chr8:30082926-30083272 | Common:2; Rare:100 | ||||
| chr8:30095360-30095515 | Common:1; Rare:49 | ||||
| chr8:30156243-30156439 | Rare:59 | ||||
| chr8:30657971-30658410 | Common:5; Rare:129 | ||||
| chr8:30727536-30727934 | Common:6; Rare:125; Clinvar (benign):1 | ||||
| chr8:30744093-30744424 | Common:4; Rare:111 | ||||
| chr8:30812809-30812931 | Common:1; Rare:51 | ||||
| chr8:32548551-32548717 | Common:1; Rare:50 | ||||
| chr8:33484628-33484747 | Rare:30 |