| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:132986236-132986433 | Rare:41 | ||||
| chr12:133130230-133130652 | Common:7; Rare:140 | ||||
| chr13:19659085-19659287 | Rare:55 | ||||
| chr13:19863491-19863937 | Common:6; Rare:170 | ||||
| chr13:19958990-19959076 | Common:1; Rare:37 | ||||
| chr13:20525756-20525975 | Common:1; Rare:78 | ||||
| chr13:20567025-20567190 | Common:1; Rare:56 | ||||
| chr13:20567452-20567770 | Common:1; Rare:72 | ||||
| chr13:21140377-21140624 | Rare:111 | ||||
| chr13:21176529-21176708 | Common:1; Rare:83 | ||||
| chr13:21603877-21603945 | Rare:39 | ||||
| chr13:21670897-21671162 | Common:1; Rare:88; Clinvar:1; Clinvar (benign):1 | ||||
| chr13:23889294-23889541 | Common:1; Rare:89 | ||||
| chr13:24160546-24160937 | Common:2; Rare:100 | ||||
| chr13:24512709-24512861 | Common:3; Rare:42 |