| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:112409554-112409707 | Common:1; Rare:52 | ||||
| chr12:113184882-113185077 | Common:1; Rare:54 | ||||
| chr12:113185429-113185800 | Common:9; Rare:134 | ||||
| chr12:113221033-113221319 | Common:2; Rare:81 | ||||
| chr12:113966306-113966506 | Common:7; Rare:67 | ||||
| chr12:114684160-114684353 | Rare:48 | ||||
| chr12:114684497-114684602 | Rare:32 | ||||
| chr12:118061059-118061407 | Common:3; Rare:80 | ||||
| chr12:118103856-118104128 | Common:1; Rare:68 | ||||
| chr12:118135931-118136218 | Common:2; Rare:91 | ||||
| chr12:118372852-118373165 | Common:2; Rare:81 | ||||
| chr12:118376333-118376568 | Common:1; Rare:68 | ||||
| chr12:119178615-119179122 | Common:2; Rare:90; Clinvar:3; Clinvar (benign):2 | ||||
| chr12:119179128-119179679 | Rare:164; Clinvar:10; Clinvar (benign):4 | ||||
| chr12:120116655-120116961 | Common:6; Rare:100 |