| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:86800193-86800274 | Common:1; Rare:18 | ||||
| chr11:86800419-86800569 | Common:1; Rare:51 | ||||
| chr11:86940594-86940740 | Rare:37 | ||||
| chr11:86941179-86941342 | Rare:28 | ||||
| chr11:86955294-86955685 | Common:1; Rare:132; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:87037492-87037895 | Common:3; Rare:139 | ||||
| chr11:87037915-87037973 | Rare:37 | ||||
| chr11:87038045-87038104 | Rare:14 | ||||
| chr11:88337380-88337430 | Common:1; Rare:18 | ||||
| chr11:88337606-88337864 | Common:4; Rare:126; Clinvar:7; Clinvar (benign):3 | ||||
| chr11:88338026-88338053 | Rare:9 | ||||
| chr11:89491264-89491365 | Common:2; Rare:31 | ||||
| chr11:89491468-89491584 | Common:2; Rare:23 | ||||
| chr11:90134472-90134532 | Rare:15 | ||||
| chr11:90134950-90135244 | Rare:57 |