| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:9575469-9575790 | Common:1; Rare:58 | ||||
| chr11:9663993-9664169 | Common:4; Rare:61 | ||||
| chr11:10304805-10305118 | Common:1; Rare:72 | ||||
| chr11:10455137-10455432 | Common:5; Rare:55; Clinvar:2; Clinvar (benign):6 | ||||
| chr11:10541128-10541321 | Common:1; Rare:72 | ||||
| chr11:10693574-10693725 | Common:1; Rare:46 | ||||
| chr11:10750697-10750994 | Common:3; Rare:78 | ||||
| chr11:10751174-10751310 | Rare:42 | ||||
| chr11:10808709-10808786 | Rare:22 | ||||
| chr11:10808864-10809263 | Common:4; Rare:170 | ||||
| chr11:10858013-10858278 | Common:3; Rare:87 | ||||
| chr11:11621460-11621518 | Rare:17 | ||||
| chr11:11841914-11842091 | Common:1; Rare:49 | ||||
| chr11:12138246-12138440 | Rare:28 | ||||
| chr11:12160694-12160985 | Common:1; Rare:53 |