| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:85627268-85627436 | Rare:30 | ||||
| chr11:85628326-85628664 | Common:7; Rare:115 | ||||
| chr11:85647851-85648067 | Common:2; Rare:58; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:86244597-86244789 | Common:1; Rare:50 | ||||
| chr11:86672141-86672223 | Rare:17 | ||||
| chr11:86955376-86955679 | Common:1; Rare:99 | ||||
| chr11:87037767-87038067 | Common:3; Rare:138 | ||||
| chr11:88337670-88337888 | Common:4; Rare:104; Clinvar:6; Clinvar (benign):3 | ||||
| chr11:90222963-90223156 | Common:2; Rare:77 | ||||
| chr11:93741381-93741723 | Common:7; Rare:137 | ||||
| chr11:93784836-93784910 | Rare:17 | ||||
| chr11:94493800-94494071 | Common:5; Rare:79; Clinvar (benign):1 | ||||
| chr11:94706439-94706571 | Common:2; Rare:31 | ||||
| chr11:94973509-94973711 | Rare:68 | ||||
| chr11:95067463-95067573 | Rare:38 |