| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:103091952-103092261 | Common:1; Rare:87 | ||||
| chr11:106077314-106077706 | Common:2; Rare:118 | ||||
| chr11:108008874-108009003 | Common:1; Rare:42 | ||||
| chr11:108009218-108009237 | Rare:4 | ||||
| chr11:108009273-108009361 | Rare:42 | ||||
| chr11:108121429-108121672 | Common:4; Rare:91; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr11:108133741-108133829 | Rare:23 | ||||
| chr11:108133992-108134315 | Common:2; Rare:64; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr11:108222526-108223128 | Common:1; Rare:197; Clinvar:8; Clinvar (benign):1 | ||||
| chr11:108223329-108223435 | Rare:30 | ||||
| chr11:108467469-108467599 | Rare:51 | ||||
| chr11:108593532-108593943 | Common:5; Rare:111 | ||||
| chr11:110429667-110429956 | Common:4; Rare:73 | ||||
| chr11:111299649-111299769 | Common:2; Rare:31 | ||||
| chr11:111379257-111379326 | Rare:9 |