| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:71663807-71664071 | Common:1; Rare:76 | ||||
| chr12:71664253-71664419 | Rare:47 | ||||
| chr12:71686026-71686120 | Common:1; Rare:25 | ||||
| chr12:71686299-71686444 | Common:1; Rare:46 | ||||
| chr12:71839623-71839775 | Common:1; Rare:55 | ||||
| chr12:74537753-74537873 | Common:1; Rare:47 | ||||
| chr12:75511578-75511744 | Rare:57 | ||||
| chr12:76084568-76084836 | Common:1; Rare:84 | ||||
| chr12:76348351-76348480 | Common:1; Rare:50; Clinvar:3; Clinvar (benign):1 | ||||
| chr12:76559715-76559924 | Rare:83 | ||||
| chr12:76763913-76764261 | Common:5; Rare:144 | ||||
| chr12:76879017-76879114 | Rare:23 | ||||
| chr12:79690528-79690678 | Rare:44 | ||||
| chr12:79934927-79935319 | Common:1; Rare:160 | ||||
| chr12:82358314-82358559 | Rare:115 |