| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:30322983-30323164 | Common:1; Rare:52 | ||||
| chr11:31369724-31369882 | Rare:48 | ||||
| chr11:31509575-31509796 | Common:1; Rare:71 | ||||
| chr11:33015784-33015935 | Common:1; Rare:59 | ||||
| chr11:33161443-33161624 | Common:5; Rare:48 | ||||
| chr11:33257621-33257737 | Rare:27 | ||||
| chr11:33258064-33258346 | Rare:98 | ||||
| chr11:33774493-33774688 | Common:2; Rare:69 | ||||
| chr11:34052126-34052470 | Common:4; Rare:160 | ||||
| chr11:34105478-34105660 | Common:2; Rare:58 | ||||
| chr11:34438777-34439000 | Common:2; Rare:75; Clinvar (benign):1 | ||||
| chr11:34620872-34621205 | Common:3; Rare:67 | ||||
| chr11:34916287-34916669 | Common:10; Rare:156; Clinvar:5; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
| chr11:35138949-35139354 | Common:1; Rare:111 | ||||
| chr11:35943936-35944110 | Common:3; Rare:59 |