| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:126113681-126113852 | Common:1; Rare:23 | ||||
| chr11:126116052-126116261 | Common:2; Rare:46 | ||||
| chr11:128334270-128334358 | Common:1; Rare:18 | ||||
| chr11:128507241-128507274 | Rare:11 | ||||
| chr11:128520686-128520719 | Rare:4 | ||||
| chr11:128586710-128586841 | Rare:27 | ||||
| chr11:128695964-128696069 | Rare:20 | ||||
| chr11:130450052-130450319 | Common:2; Rare:59 | ||||
| chr11:130477748-130477957 | Common:3; Rare:32 | ||||
| chr11:130519589-130519820 | Common:3; Rare:53 | ||||
| chr11:134037291-134037347 | Rare:24 | ||||
| chr12:16762-17034 | Common:9; Rare:78 | ||||
| chr12:753858-754306 | Common:2; Rare:150; Clinvar:8; Clinvar (benign):6 | ||||
| chr12:2264968-2265178 | Rare:38 | ||||
| chr12:2457987-2458281 | Common:4; Rare:55 |