| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:118061095-118061468 | Common:8; Rare:143 | ||||
| chr12:118062340-118062860 | Common:10; Rare:182 | ||||
| chr12:118103689-118104108 | Common:2; Rare:167 | ||||
| chr12:118135912-118136190 | Common:4; Rare:157 | ||||
| chr12:118372820-118373246 | Common:5; Rare:227 | ||||
| chr12:118376100-118376630 | Common:2; Rare:220 | ||||
| chr12:119178627-119178965 | Common:1; Rare:62; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:119667451-119668129 | Common:5; Rare:243 | ||||
| chr12:119668093-119668222 | Common:1; Rare:30 | ||||
| chr12:119877258-119877572 | Common:4; Rare:143 | ||||
| chr12:119989530-119989860 | Common:4; Rare:211 | ||||
| chr12:120116687-120117011 | Common:12; Rare:230 | ||||
| chr12:120117060-120117550 | Common:6; Rare:245 | ||||
| chr12:120194672-120194813 | Common:1; Rare:98 | ||||
| chr12:120201069-120201391 | Common:2; Rare:102 |