| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:118103677-118104164 | Common:2; Rare:116 | ||||
| chr12:118135932-118136204 | Common:2; Rare:84 | ||||
| chr12:118372817-118373284 | Common:3; Rare:136 | ||||
| chr12:118376199-118376638 | Common:1; Rare:128 | ||||
| chr12:118376820-118376923 | Rare:31 | ||||
| chr12:119178615-119179031 | Common:1; Rare:71; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:119179664-119179874 | Common:1; Rare:49 | ||||
| chr12:119334549-119334757 | Common:1; Rare:43 | ||||
| chr12:119667792-119667926 | Common:1; Rare:39 | ||||
| chr12:119667928-119668180 | Common:2; Rare:63 | ||||
| chr12:119669889-119669931 | Common:1; Rare:8 | ||||
| chr12:119877230-119877606 | Common:3; Rare:82 | ||||
| chr12:120116322-120116451 | Rare:29 | ||||
| chr12:120116594-120117060 | Common:9; Rare:142 | ||||
| chr12:120117108-120117511 | Common:3; Rare:117 |