| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:122416039-122416237 | Common:1; Rare:62 | ||||
| chr3:122514761-122515026 | Common:3; Rare:74 | ||||
| chr3:122564181-122564225 | Rare:11 | ||||
| chr3:122564230-122564504 | Common:4; Rare:80 | ||||
| chr3:122680701-122680970 | Rare:84 | ||||
| chr3:122680999-122681063 | Rare:11 | ||||
| chr3:123201625-123202010 | Common:1; Rare:103 | ||||
| chr3:123404547-123404813 | Common:1; Rare:56 | ||||
| chr3:123585028-123585319 | Common:1; Rare:90 | ||||
| chr3:123585489-123585648 | Rare:28 | ||||
| chr3:123620205-123620597 | Common:1; Rare:88; Clinvar:5 | ||||
| chr3:123649133-123649288 | Common:2; Rare:47; Clinvar:1; Clinvar (benign):10 | ||||
| chr3:123692335-123692476 | Rare:31 | ||||
| chr3:123700936-123701321 | Rare:82; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:123701436-123701583 | Common:1; Rare:49; Clinvar:7 |