| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:119240873-119241129 | Common:1; Rare:69 | ||||
| chr3:119463598-119463780 | Common:3; Rare:52 | ||||
| chr3:119498409-119498651 | Common:4; Rare:81 | ||||
| chr3:119579402-119579826 | Common:4; Rare:107 | ||||
| chr3:119677372-119677469 | Rare:30 | ||||
| chr3:120093675-120093763 | Rare:28 | ||||
| chr3:120742508-120742822 | Common:2; Rare:86 | ||||
| chr3:121660821-121661027 | Rare:41 | ||||
| chr3:121749646-121750036 | Common:1; Rare:90 | ||||
| chr3:121834970-121835264 | Common:3; Rare:99; Clinvar:6; Clinvar (benign):2 | ||||
| chr3:122416002-122416225 | Common:1; Rare:75 | ||||
| chr3:122564221-122564429 | Common:3; Rare:59 | ||||
| chr3:122793699-122793963 | Common:3; Rare:73 | ||||
| chr3:122794724-122794825 | Rare:15 | ||||
| chr3:122794971-122795069 | Rare:33 |