| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:111766722-111766977 | Rare:70 | ||||
| chr12:111841877-111842224 | Common:3; Rare:94 | ||||
| chr12:112013125-112013468 | Common:1; Rare:121 | ||||
| chr12:113185456-113185755 | Common:7; Rare:108 | ||||
| chr12:113966315-113966536 | Common:9; Rare:77 | ||||
| chr12:117190322-117190561 | Common:1; Rare:99 | ||||
| chr12:118061071-118061407 | Common:3; Rare:75 | ||||
| chr12:118135941-118136195 | Common:2; Rare:79 | ||||
| chr12:118372827-118373165 | Common:2; Rare:88 | ||||
| chr12:118376256-118376576 | Common:1; Rare:93 | ||||
| chr12:118981285-118981568 | Common:1; Rare:81 | ||||
| chr12:120116720-120116911 | Rare:58 | ||||
| chr12:120194693-120194786 | Rare:34 | ||||
| chr12:120201085-120201366 | Common:2; Rare:88 | ||||
| chr12:120438018-120438139 | Rare:44; Clinvar (benign):1 |