| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:122564264-122564428 | Common:1; Rare:50 | ||||
| chr3:123585043-123585284 | Common:1; Rare:74 | ||||
| chr3:124730377-124730468 | Common:2; Rare:48; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:125375255-125375389 | Rare:34 | ||||
| chr3:127598217-127598446 | Common:3; Rare:63 | ||||
| chr3:128123767-128124026 | Rare:68 | ||||
| chr3:128879404-128879665 | Common:4; Rare:124; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:129161027-129161168 | Common:1; Rare:54 | ||||
| chr3:129249545-129249664 | Common:1; Rare:35 | ||||
| chr3:129439916-129440247 | Common:1; Rare:98; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:134485969-134486253 | Common:3; Rare:97 | ||||
| chr3:136752368-136752671 | Common:1; Rare:107 | ||||
| chr3:136862069-136862277 | Rare:56 | ||||
| chr3:138594209-138594521 | Rare:102 | ||||
| chr3:139389617-139389825 | Common:1; Rare:63 |