| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:124863593-124864123 | Common:5; Rare:147 | ||||
| chr12:124914549-124915057 | Common:9; Rare:213 | ||||
| chr12:125065319-125065492 | Common:1; Rare:62 | ||||
| chr12:130716266-130716525 | Rare:40 | ||||
| chr12:130871771-130872122 | Common:4; Rare:140 | ||||
| chr12:131710839-131711138 | Common:1; Rare:77 | ||||
| chr12:131929002-131929296 | Common:10; Rare:88; Clinvar:1 | ||||
| chr12:132687303-132687659 | Common:2; Rare:131; Clinvar:7; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr12:132710730-132711035 | Common:4; Rare:100 | ||||
| chr12:132828809-132829181 | Common:4; Rare:130 | ||||
| chr12:132887553-132887859 | Rare:91 | ||||
| chr12:132956243-132956410 | Common:1; Rare:39 | ||||
| chr12:132986291-132986442 | Rare:34 | ||||
| chr12:133037213-133037539 | Common:4; Rare:67 | ||||
| chr12:133080217-133080459 | Common:6; Rare:71 |