| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:123601803-123602153 | Common:6; Rare:93 | ||||
| chr12:123633546-123633851 | Common:1; Rare:145; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:123972545-123972929 | Common:6; Rare:128 | ||||
| chr12:124863847-124864105 | Common:1; Rare:75 | ||||
| chr12:131710795-131711116 | Rare:86 | ||||
| chr12:131929076-131929491 | Common:9; Rare:114; Clinvar:5 | ||||
| chr12:132144306-132144490 | Rare:74 | ||||
| chr12:132687311-132687655 | Common:2; Rare:128; Clinvar:5; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr12:132761797-132762117 | Common:3; Rare:107 | ||||
| chr12:132887542-132887839 | Rare:92 | ||||
| chr12:132956243-132956370 | Common:1; Rare:32 | ||||
| chr12:133130231-133130645 | Common:7; Rare:134 | ||||
| chr13:19633517-19633778 | Common:1; Rare:100 | ||||
| chr13:19782921-19783074 | Common:1; Rare:54 | ||||
| chr13:19863457-19863956 | Common:6; Rare:179 |