| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:124423050-124423332 | Common:2; Rare:71 | ||||
| chr12:124914567-124915066 | Common:9; Rare:207 | ||||
| chr12:131710788-131711107 | Rare:85 | ||||
| chr12:132687311-132687662 | Common:2; Rare:129; Clinvar:5; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr12:132710564-132710842 | Common:4; Rare:101 | ||||
| chr12:132887553-132887775 | Rare:72 | ||||
| chr12:132956252-132956383 | Common:1; Rare:31 | ||||
| chr12:133080732-133080953 | Rare:68 | ||||
| chr12:133130238-133130652 | Common:7; Rare:137 | ||||
| chr13:19633454-19633746 | Common:1; Rare:112 | ||||
| chr13:19863481-19863870 | Common:5; Rare:140 | ||||
| chr13:20566818-20567202 | Common:1; Rare:111 | ||||
| chr13:21140352-21140624 | Rare:121 | ||||
| chr13:21176545-21176859 | Common:3; Rare:129 | ||||
| chr13:23889306-23889460 | Rare:53 |