| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:85647824-85648088 | Common:2; Rare:71; Clinvar:3; Clinvar (benign):2 | ||||
| chr11:85663898-85664180 | Common:2; Rare:66 | ||||
| chr11:85718182-85718299 | Common:1; Rare:23 | ||||
| chr11:85718902-85718933 | Rare:10 | ||||
| chr11:86302084-86302478 | Common:3; Rare:87 | ||||
| chr11:86800361-86800608 | Common:1; Rare:92 | ||||
| chr11:86955391-86955623 | Common:1; Rare:71 | ||||
| chr11:88337654-88337924 | Common:5; Rare:124; Clinvar:6; Clinvar (benign):3 | ||||
| chr11:90223015-90223160 | Common:1; Rare:53 | ||||
| chr11:93741330-93741702 | Common:8; Rare:146 | ||||
| chr11:93784182-93784347 | Common:3; Rare:55 | ||||
| chr11:94129050-94129280 | Common:2; Rare:66 | ||||
| chr11:94493780-94494025 | Common:4; Rare:71; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:94970088-94970257 | Rare:34 | ||||
| chr11:94973539-94973711 | Rare:52 |