| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:6320490-6320623 | Common:2; Rare:45 | ||||
| chr11:6390237-6390532 | Common:2; Rare:87 | ||||
| chr11:6473889-6474144 | Rare:74 | ||||
| chr11:6481304-6481524 | Common:4; Rare:87 | ||||
| chr11:6603536-6603822 | Common:4; Rare:89; Clinvar (benign):3 | ||||
| chr11:6683261-6683634 | Common:6; Rare:144 | ||||
| chr11:7020305-7020462 | Rare:50 | ||||
| chr11:7965396-7965741 | Common:2; Rare:49 | ||||
| chr11:8682650-8683021 | Common:2; Rare:157 | ||||
| chr11:8964366-8964531 | Common:4; Rare:53 | ||||
| chr11:8964931-8965020 | Common:1; Rare:21 | ||||
| chr11:9575366-9575541 | Common:2; Rare:27 | ||||
| chr11:9663893-9664249 | Common:4; Rare:119 | ||||
| chr11:10304806-10305150 | Common:1; Rare:79 | ||||
| chr11:10455125-10455145 | Common:1; Clinvar (benign):1 |