| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:77940082-77940403 | Common:2; Rare:65 | ||||
| chr12:78863669-78864029 | Common:1; Rare:68 | ||||
| chr12:78864375-78864884 | Common:3; Rare:109 | ||||
| chr12:79690460-79690603 | Rare:36 | ||||
| chr12:79690605-79690646 | Rare:13 | ||||
| chr12:79690924-79691207 | Rare:89 | ||||
| chr12:79788723-79789007 | Rare:75 | ||||
| chr12:79934882-79935399 | Common:1; Rare:193 | ||||
| chr12:82358222-82358566 | Common:2; Rare:171 | ||||
| chr12:82358716-82358899 | Common:3; Rare:97 | ||||
| chr12:85036249-85036368 | Rare:29 | ||||
| chr12:85836199-85836259 | Common:1; Rare:17 | ||||
| chr12:85836300-85836491 | Common:1; Rare:24 | ||||
| chr12:88141871-88142431 | Common:1; Rare:147; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:88580386-88580569 | Common:2; Rare:59 |