| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:121749464-121749536 | Rare:13 | ||||
| chr3:121749633-121750025 | Common:1; Rare:90 | ||||
| chr3:121834956-121835244 | Common:3; Rare:95; Clinvar:6; Clinvar (benign):2 | ||||
| chr3:122383192-122383323 | Common:1; Rare:41 | ||||
| chr3:122384063-122384258 | Rare:71 | ||||
| chr3:122416039-122416226 | Common:1; Rare:61 | ||||
| chr3:122514834-122515031 | Common:2; Rare:56 | ||||
| chr3:122564236-122564429 | Common:3; Rare:57 | ||||
| chr3:122680790-122680874 | Rare:32 | ||||
| chr3:123585028-123585272 | Common:1; Rare:79 | ||||
| chr3:123585490-123585590 | Rare:19 | ||||
| chr3:123620418-123620689 | Common:3; Rare:39 | ||||
| chr3:123692349-123692468 | Rare:28 | ||||
| chr3:123700957-123701302 | Rare:72; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:123701436-123701688 | Common:1; Rare:71; Clinvar:7 |