| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:97183186-97183536 | Common:4; Rare:128 | ||||
| chr5:98773430-98773666 | Common:4; Rare:58 | ||||
| chr5:98928903-98929196 | Common:4; Rare:128 | ||||
| chr5:100535232-100535599 | Rare:102 | ||||
| chr5:100903207-100903389 | Common:1; Rare:33 | ||||
| chr5:103120072-103120393 | Common:1; Rare:77 | ||||
| chr5:103562493-103562564 | Common:1; Rare:22 | ||||
| chr5:108382054-108382167 | Common:1; Rare:39 | ||||
| chr5:108748679-108748991 | Common:2; Rare:107 | ||||
| chr5:109409842-109410249 | Common:4; Rare:155 | ||||
| chr5:110738915-110739128 | Common:2; Rare:87 | ||||
| chr5:111224345-111224496 | Rare:70 | ||||
| chr5:111512431-111512634 | Common:3; Rare:85 | ||||
| chr5:111757146-111757261 | Common:5; Rare:21 | ||||
| chr5:112707703-112707817 | Rare:43; Clinvar:18; Clinvar (benign):3 |