| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:113746108-113746328 | Common:1; Rare:84 | ||||
| chr3:113746773-113747071 | Common:4; Rare:65 | ||||
| chr3:114056481-114056816 | Common:2; Rare:129 | ||||
| chr3:115100218-115100399 | Rare:28 | ||||
| chr3:120742503-120742771 | Common:2; Rare:75 | ||||
| chr3:121749711-121750021 | Common:1; Rare:70 | ||||
| chr3:121834977-121835265 | Common:3; Rare:97; Clinvar:6; Clinvar (benign):2 | ||||
| chr3:122383194-122383334 | Common:1; Rare:41 | ||||
| chr3:122384084-122384268 | Rare:68 | ||||
| chr3:122416068-122416225 | Rare:47 | ||||
| chr3:122564252-122564419 | Common:2; Rare:50 | ||||
| chr3:123585063-123585406 | Common:2; Rare:101 | ||||
| chr3:123585489-123585553 | Rare:11 | ||||
| chr3:125375237-125375388 | Rare:41 | ||||
| chr3:126084110-126084304 | Common:1; Rare:81 |