| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:110468667-110468944 | Rare:78 | ||||
| chr12:110496186-110496288 | Common:1; Rare:19 | ||||
| chr12:110502037-110502340 | Common:1; Rare:112 | ||||
| chr12:110613991-110614220 | Rare:72; Clinvar:3; Clinvar (benign):2 | ||||
| chr12:111599338-111599635 | Common:2; Rare:97 | ||||
| chr12:111685761-111686127 | Rare:136 | ||||
| chr12:111841835-111842000 | Common:2; Rare:53 | ||||
| chr12:112013104-112013468 | Common:1; Rare:132 | ||||
| chr12:112108718-112108813 | Rare:24 | ||||
| chr12:112109432-112109473 | Rare:4 | ||||
| chr12:112409141-112409197 | Rare:8 | ||||
| chr12:112409493-112409707 | Common:1; Rare:71 | ||||
| chr12:113185435-113185754 | Common:7; Rare:120 | ||||
| chr12:113422309-113422417 | Common:1; Rare:28 | ||||
| chr12:113966286-113966547 | Common:9; Rare:88 |