| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:102452502-102452949 | Common:2; Rare:148 | ||||
| chr11:102453019-102453175 | Rare:39 | ||||
| chr11:102530645-102530663 | Rare:11 | ||||
| chr11:103091925-103092248 | Common:1; Rare:88 | ||||
| chr11:106022211-106022546 | Common:3; Rare:96 | ||||
| chr11:106077289-106077711 | Common:2; Rare:128 | ||||
| chr11:107457753-107457940 | Common:2; Rare:64 | ||||
| chr11:108008838-108009061 | Common:1; Rare:62 | ||||
| chr11:108009111-108009212 | Rare:24 | ||||
| chr11:108009254-108009369 | Rare:53 | ||||
| chr11:108121419-108121608 | Common:3; Rare:67; Clinvar:1; Clinvar (benign):4 | ||||
| chr11:108134016-108134315 | Common:2; Rare:61; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr11:108222544-108223133 | Common:1; Rare:190; Clinvar:8; Clinvar (benign):1 | ||||
| chr11:108223307-108223441 | Rare:39 | ||||
| chr11:108223955-108224075 | Rare:29 |