| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:119468817-119469007 | Rare:67 | ||||
| chr3:119498409-119498759 | Common:4; Rare:112 | ||||
| chr3:120742494-120742832 | Common:2; Rare:92 | ||||
| chr3:121834966-121835237 | Common:3; Rare:85; Clinvar:6; Clinvar (benign):2 | ||||
| chr3:122384036-122384281 | Common:3; Rare:86 | ||||
| chr3:122416002-122416227 | Common:1; Rare:75 | ||||
| chr3:122564238-122564594 | Common:4; Rare:104 | ||||
| chr3:122795000-122795118 | Common:1; Rare:57 | ||||
| chr3:123585020-123585284 | Common:1; Rare:85 | ||||
| chr3:123620204-123620636 | Common:1; Rare:94; Clinvar:5 | ||||
| chr3:123700979-123701229 | Rare:50; Clinvar:3; Clinvar (benign):1 | ||||
| chr3:123949589-123949602 | Rare:1 | ||||
| chr3:123949620-123949683 | Rare:11 | ||||
| chr3:123949701-123949799 | Common:1; Rare:17 | ||||
| chr3:123961188-123961503 | Common:3; Rare:124 |