| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:114179647-114179816 | Rare:25 | ||||
| chr11:114366944-114367169 | Common:2; Rare:38 | ||||
| chr11:117289684-117290019 | Rare:84 | ||||
| chr11:117290567-117290917 | Common:2; Rare:82 | ||||
| chr11:118791693-118791825 | Rare:41 | ||||
| chr11:122100537-122100830 | Common:4; Rare:55 | ||||
| chr11:122102106-122102189 | Rare:18 | ||||
| chr11:122180392-122180632 | Common:1; Rare:31 | ||||
| chr12:3211913-3211933 | Common:1; Rare:4 | ||||
| chr12:6614142-6614388 | Rare:63 | ||||
| chr12:7088608-7088935 | Common:1; Rare:101; Clinvar (pathogenic):2 | ||||
| chr12:8242933-8243245 | Common:8; Rare:88 | ||||
| chr12:9240318-9240394 | Common:1; Rare:16 | ||||
| chr12:9283884-9284034 | Common:4; Rare:9 | ||||
| chr12:9448179-9448328 | Common:1; Rare:74 |