| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:114624930-114625017 | Rare:14 | ||||
| chr3:119463604-119463817 | Common:3; Rare:63 | ||||
| chr3:119468734-119469010 | Rare:83 | ||||
| chr3:120094414-120094771 | Common:4; Rare:113 | ||||
| chr3:120596130-120596448 | Common:2; Rare:122 | ||||
| chr3:120742503-120742777 | Common:2; Rare:77 | ||||
| chr3:121545941-121546028 | Rare:26 | ||||
| chr3:121660869-121661028 | Rare:24 | ||||
| chr3:121749711-121750021 | Common:1; Rare:70 | ||||
| chr3:121834987-121835231 | Common:3; Rare:81; Clinvar:6; Clinvar (benign):2 | ||||
| chr3:122383190-122383323 | Common:1; Rare:42 | ||||
| chr3:122384117-122384247 | Rare:52 | ||||
| chr3:122416068-122416203 | Rare:39 | ||||
| chr3:122514873-122515023 | Common:1; Rare:41 | ||||
| chr3:122564244-122564437 | Common:3; Rare:58 |