| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:51026313-51026488 | Common:2; Rare:84; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:51048111-51048370 | Common:2; Rare:92 | ||||
| chr12:51173074-51173235 | Rare:28 | ||||
| chr12:51238620-51238914 | Common:8; Rare:120 | ||||
| chr12:51239154-51239317 | Common:1; Rare:43 | ||||
| chr12:51424660-51425006 | Common:2; Rare:85 | ||||
| chr12:51590741-51590975 | Common:1; Rare:71 | ||||
| chr12:51951468-51951745 | Common:4; Rare:107 | ||||
| chr12:52051152-52051471 | Common:1; Rare:106 | ||||
| chr12:52069679-52070030 | Common:1; Rare:115 | ||||
| chr12:53006125-53006495 | Common:4; Rare:134 | ||||
| chr12:53054390-53054572 | Common:1; Rare:65 | ||||
| chr12:53079329-53079559 | Common:2; Rare:78 | ||||
| chr12:53097285-53097402 | Common:1; Rare:20 | ||||
| chr12:53097442-53098233 | Common:2; Rare:203 |