| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:102047343-102047480 | Common:1; Rare:48 | ||||
| chr11:102347131-102347317 | Common:2; Rare:67 | ||||
| chr11:102451858-102451995 | Rare:36 | ||||
| chr11:102452591-102452943 | Common:2; Rare:112 | ||||
| chr11:103091997-103092278 | Common:2; Rare:89 | ||||
| chr11:103109324-103109571 | Common:1; Rare:68; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:104164086-104164147 | Rare:10 | ||||
| chr11:105610462-105610780 | Common:1; Rare:75 | ||||
| chr11:106022172-106022556 | Common:3; Rare:112 | ||||
| chr11:106077306-106077808 | Common:2; Rare:165 | ||||
| chr11:107591031-107591376 | Common:3; Rare:111 | ||||
| chr11:107859172-107859489 | Common:1; Rare:59 | ||||
| chr11:108008792-108009187 | Common:1; Rare:100 | ||||
| chr11:108009255-108009370 | Rare:53 | ||||
| chr11:108121419-108121653 | Common:4; Rare:85; Clinvar:1; Clinvar (benign):5 |