| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:96389862-96390043 | Common:1; Rare:72 | ||||
| chr11:102317201-102317489 | Rare:49 | ||||
| chr11:102347076-102347354 | Common:4; Rare:87 | ||||
| chr11:106077340-106077711 | Common:2; Rare:114 | ||||
| chr11:108009292-108009351 | Rare:31 | ||||
| chr11:108222594-108223108 | Common:1; Rare:165; Clinvar:7; Clinvar (benign):1 | ||||
| chr11:110296494-110296802 | Common:2; Rare:138; Clinvar:8 | ||||
| chr11:111766369-111766439 | Common:1; Rare:42 | ||||
| chr11:112086722-112086921 | Rare:84; Clinvar:3; Clinvar (pathogenic):2 | ||||
| chr11:112226314-112226446 | Rare:61 | ||||
| chr11:113314448-113314588 | Rare:48 | ||||
| chr11:113875497-113875768 | Common:4; Rare:100 | ||||
| chr11:114400412-114400753 | Common:2; Rare:134 | ||||
| chr11:117144204-117144393 | Common:2; Rare:91 | ||||
| chr11:117199018-117199411 | Common:6; Rare:125 |