| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:155854364-155854752 | Rare:108 | ||||
| chr3:155870323-155870743 | Common:2; Rare:119 | ||||
| chr3:156555043-156555409 | Common:2; Rare:141 | ||||
| chr3:156674420-156674618 | Common:2; Rare:49 | ||||
| chr3:157159866-157159879 | Rare:2 | ||||
| chr3:157160090-157160334 | Rare:101 | ||||
| chr3:158644504-158644644 | Common:4; Rare:55; Clinvar (benign):5 | ||||
| chr3:158801993-158802146 | Common:2; Rare:73 | ||||
| chr3:159839938-159839974 | Rare:6 | ||||
| chr3:160399164-160399311 | Rare:39; Clinvar:2 | ||||
| chr3:160399482-160399687 | Rare:57; Clinvar:2 | ||||
| chr3:160449748-160450018 | Common:2; Rare:82 | ||||
| chr3:160565528-160565778 | Common:2; Rare:98 | ||||
| chr3:161221162-161221394 | Common:2; Rare:74 | ||||
| chr3:161371462-161371521 | Common:1; Rare:10 |