| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:116832289-116832516 | Common:1; Rare:44 | ||||
| chr11:117191733-117191965 | Common:1; Rare:70 | ||||
| chr11:117289790-117289824 | Rare:10 | ||||
| chr11:119094708-119094888 | Common:1; Rare:54 | ||||
| chr11:119335742-119335829 | Rare:17 | ||||
| chr11:120337721-120337850 | Common:1; Rare:22 | ||||
| chr11:121569830-121570034 | Rare:58 | ||||
| chr11:125614188-125614426 | Rare:59; Clinvar (benign):1 | ||||
| chr11:126327415-126327604 | Common:1; Rare:36 | ||||
| chr12:578003-578246 | Common:1; Rare:46 | ||||
| chr12:753868-754003 | Common:1; Rare:59; Clinvar:3; Clinvar (benign):1 | ||||
| chr12:754021-754186 | Rare:60; Clinvar:4; Clinvar (benign):1 | ||||
| chr12:1669106-1669381 | Common:2; Rare:58 | ||||
| chr12:6770156-6770569 | Rare:115 | ||||
| chr12:7088608-7089001 | Common:2; Rare:119; Clinvar (pathogenic):2 |