| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:113515120-113515275 | Rare:50 | ||||
| chr3:113745958-113746033 | Common:1; Rare:24 | ||||
| chr3:113746052-113746383 | Common:1; Rare:122 | ||||
| chr3:113746778-113747076 | Common:4; Rare:67 | ||||
| chr3:114056492-114056816 | Common:2; Rare:124 | ||||
| chr3:119468843-119469018 | Rare:68 | ||||
| chr3:119498431-119498609 | Common:3; Rare:64 | ||||
| chr3:120742503-120742782 | Common:2; Rare:78 | ||||
| chr3:121749631-121750011 | Common:1; Rare:87 | ||||
| chr3:121834986-121835231 | Common:3; Rare:81; Clinvar:6; Clinvar (benign):2 | ||||
| chr3:122383192-122383323 | Common:1; Rare:41 | ||||
| chr3:122384063-122384243 | Rare:67 | ||||
| chr3:122416039-122416219 | Common:1; Rare:59 | ||||
| chr3:122564243-122564447 | Common:3; Rare:63 | ||||
| chr3:123066940-123067146 | Rare:54 |