| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:120742503-120742777 | Common:2; Rare:77 | ||||
| chr3:120908093-120908249 | Rare:46 | ||||
| chr3:121749643-121750021 | Common:1; Rare:87 | ||||
| chr3:121834983-121835248 | Common:3; Rare:91; Clinvar:6; Clinvar (benign):2 | ||||
| chr3:122383192-122383351 | Common:2; Rare:48 | ||||
| chr3:122384054-122384243 | Rare:71 | ||||
| chr3:122416039-122416227 | Common:1; Rare:61 | ||||
| chr3:122514822-122515031 | Common:2; Rare:60 | ||||
| chr3:122564236-122564426 | Common:3; Rare:55 | ||||
| chr3:123201838-123201967 | Common:1; Rare:41 | ||||
| chr3:123585035-123585317 | Common:1; Rare:85 | ||||
| chr3:123585460-123585553 | Rare:17 | ||||
| chr3:123620205-123620602 | Common:1; Rare:89; Clinvar:5 | ||||
| chr3:123692353-123692468 | Rare:24 | ||||
| chr3:123700936-123701218 | Rare:63; Clinvar:4; Clinvar (benign):1 |