| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:197791113-197791281 | Common:2; Rare:57 | ||||
| chr3:197949885-197950270 | Common:4; Rare:114; Clinvar (benign):2 | ||||
| chr3:197959979-197960255 | Common:1; Rare:96 | ||||
| chr4:53094-53383 | Rare:5 | ||||
| chr4:124342-124564 | Common:5; Rare:64 | ||||
| chr4:124702-124798 | Common:2; Rare:23 | ||||
| chr4:337403-337879 | Common:4; Rare:138 | ||||
| chr4:474077-474351 | Common:3; Rare:98 | ||||
| chr4:499102-499319 | Common:3; Rare:87 | ||||
| chr4:663616-663759 | Rare:51 | ||||
| chr4:674212-674521 | Common:1; Rare:138 | ||||
| chr4:932259-932520 | Common:2; Rare:103 | ||||
| chr4:1289650-1289931 | Common:1; Rare:97 | ||||
| chr4:1309361-1309641 | Common:3; Rare:72 | ||||
| chr4:1721261-1721576 | Common:6; Rare:101 |