| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:102478536-102478572 | Rare:11 | ||||
| chr12:102480448-102480584 | Rare:16 | ||||
| chr12:102917231-102917320 | Common:1; Rare:29; Clinvar (benign):1 | ||||
| chr12:102950736-102950967 | Common:3; Rare:53 | ||||
| chr12:102951110-102951276 | Common:1; Rare:34 | ||||
| chr12:103495917-103496021 | Common:4; Rare:25 | ||||
| chr12:103802408-103802609 | Common:3; Rare:25 | ||||
| chr12:103841253-103841466 | Common:3; Rare:71 | ||||
| chr12:103929944-103930585 | Common:9; Rare:201 | ||||
| chr12:103937557-103937805 | Rare:55 | ||||
| chr12:103957133-103957259 | Common:2; Rare:35 | ||||
| chr12:103965664-103965960 | Common:2; Rare:74 | ||||
| chr12:104064126-104064458 | Common:3; Rare:66 | ||||
| chr12:104064459-104064628 | Rare:48 | ||||
| chr12:104065201-104065277 | Rare:12 |