| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:101950316-101950576 | Rare:43 | ||||
| chr11:102401718-102401730 | Rare:5 | ||||
| chr11:102426859-102426968 | Rare:35 | ||||
| chr11:103066301-103066463 | Common:1; Rare:22 | ||||
| chr11:108935255-108935408 | Rare:24 | ||||
| chr11:109940874-109941013 | Common:1; Rare:21 | ||||
| chr11:112078087-112078298 | Rare:46 | ||||
| chr11:112151897-112151922 | Rare:4 | ||||
| chr11:114447293-114447356 | Rare:19 | ||||
| chr11:115481255-115481364 | Rare:20 | ||||
| chr11:117166100-117166203 | Rare:28 | ||||
| chr11:117211843-117212174 | Common:2; Rare:66 | ||||
| chr11:118926218-118926319 | Common:3; Rare:19 | ||||
| chr11:119043961-119044209 | Common:2; Rare:37 | ||||
| chr11:119090023-119090266 | Rare:62; Clinvar:1; Clinvar (pathogenic):3 |