| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:114624930-114625024 | Common:1; Rare:14 | ||||
| chr3:115100267-115100399 | Rare:21 | ||||
| chr3:119463598-119463817 | Common:3; Rare:66 | ||||
| chr3:119468843-119469018 | Rare:68 | ||||
| chr3:119677322-119677517 | Common:1; Rare:70 | ||||
| chr3:120094429-120094771 | Common:4; Rare:108 | ||||
| chr3:120742503-120742777 | Common:2; Rare:77 | ||||
| chr3:121749131-121749278 | Rare:25 | ||||
| chr3:121749467-121749522 | Rare:10 | ||||
| chr3:121749633-121749994 | Common:1; Rare:82 | ||||
| chr3:121834987-121835248 | Common:3; Rare:91; Clinvar:6; Clinvar (benign):2 | ||||
| chr3:122383184-122383345 | Common:2; Rare:48 | ||||
| chr3:122384036-122384258 | Rare:80 | ||||
| chr3:122416049-122416225 | Rare:57 | ||||
| chr3:122514880-122515031 | Common:1; Rare:38 |