| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:112318393-112318527 | Common:1; Rare:18 | ||||
| chr11:113184624-113184767 | Rare:22 | ||||
| chr11:113190314-113190658 | Common:2; Rare:61 | ||||
| chr11:113384649-113384820 | Rare:27 | ||||
| chr11:113384843-113384973 | Common:1; Rare:23 | ||||
| chr11:113401758-113402022 | Common:7; Rare:43 | ||||
| chr11:113446262-113446531 | Common:2; Rare:50 | ||||
| chr11:113690714-113690908 | Common:1; Rare:49; Clinvar (benign):1 | ||||
| chr11:113778164-113778230 | Rare:14 | ||||
| chr11:113874863-113874896 | Common:1; Rare:5 | ||||
| chr11:114036217-114036563 | Common:2; Rare:80 | ||||
| chr11:114080445-114080616 | Common:1; Rare:29 | ||||
| chr11:114154400-114154897 | Common:2; Rare:76 | ||||
| chr11:114159314-114159494 | Rare:35 | ||||
| chr11:114160031-114160374 | Common:3; Rare:69 |