| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:114161164-114161337 | Common:3; Rare:28 | ||||
| chr11:114162860-114162897 | Rare:11 | ||||
| chr11:114166987-114167289 | Common:17; Rare:85 | ||||
| chr11:114178836-114179135 | Common:3; Rare:46 | ||||
| chr11:114179201-114179251 | Rare:5 | ||||
| chr11:114179644-114179828 | Common:1; Rare:27 | ||||
| chr11:114194120-114194322 | Common:2; Rare:41 | ||||
| chr11:118791680-118791751 | Common:1; Rare:17 | ||||
| chr11:119312050-119312359 | Common:1; Rare:106 | ||||
| chr11:119314491-119314716 | Common:1; Rare:75 | ||||
| chr11:122100423-122100733 | Common:4; Rare:71 | ||||
| chr11:123431030-123431139 | Rare:33 | ||||
| chr11:130914803-130915095 | Common:5; Rare:95 | ||||
| chr12:642723-643012 | Common:3; Rare:86 | ||||
| chr12:753867-754007 | Common:1; Rare:61; Clinvar:3; Clinvar (benign):1 |