| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:117232010-117232238 | Rare:127 | ||||
| chr11:117232360-117232780 | Common:8; Rare:270 | ||||
| chr11:117316202-117316419 | Common:1; Rare:51 | ||||
| chr11:117327451-117328226 | Common:10; Rare:324 | ||||
| chr11:117876532-117877166 | Common:10; Rare:283 | ||||
| chr11:117929317-117929548 | Common:10; Rare:106 | ||||
| chr11:117986150-117986530 | Common:9; Rare:210; Clinvar:4; Clinvar (benign):1 | ||||
| chr11:117994675-117994877 | Common:2; Rare:29 | ||||
| chr11:118076791-118077123 | Common:10; Rare:193 | ||||
| chr11:118142855-118143015 | Common:1; Rare:37 | ||||
| chr11:118251933-118252463 | Common:2; Rare:290 | ||||
| chr11:118263785-118263925 | Common:1; Rare:22 | ||||
| chr11:118264200-118264505 | Common:3; Rare:152 | ||||
| chr11:118359363-118359706 | Common:9; Rare:270 | ||||
| chr11:118401027-118401733 | Common:2; Rare:485 |