| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:114056500-114056817 | Common:2; Rare:123 | ||||
| chr3:119498409-119498769 | Common:4; Rare:115 | ||||
| chr3:120742501-120742789 | Common:2; Rare:81 | ||||
| chr3:121749643-121749904 | Rare:59 | ||||
| chr3:121834970-121835237 | Common:3; Rare:84; Clinvar:6; Clinvar (benign):2 | ||||
| chr3:122383180-122383305 | Common:1; Rare:41 | ||||
| chr3:122416002-122416226 | Common:1; Rare:75 | ||||
| chr3:122564239-122564421 | Common:3; Rare:53 | ||||
| chr3:123585517-123585560 | Rare:7 | ||||
| chr3:123692335-123692500 | Rare:39 | ||||
| chr3:125520153-125520287 | Rare:46 | ||||
| chr3:126083982-126084189 | Common:2; Rare:61 | ||||
| chr3:127598233-127598458 | Common:3; Rare:63 | ||||
| chr3:127822484-127822611 | Rare:32 | ||||
| chr3:128052175-128052553 | Common:2; Rare:131 |