| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65440515-65440781 | Common:2; Rare:42 | ||||
| chr11:65499039-65499943 | Common:5; Rare:531 | ||||
| chr11:65501201-65501249 | Common:2; Rare:25 | ||||
| chr11:65501807-65502115 | Common:1; Rare:135 | ||||
| chr11:65504532-65504633 | Rare:45 | ||||
| chr11:65504818-65504855 | Rare:20 | ||||
| chr11:65891205-65891504 | Common:1; Rare:71 | ||||
| chr11:89178647-89178725 | Rare:29; Clinvar:3; Clinvar (pathogenic):2 | ||||
| chr11:94129472-94129530 | Common:1; Rare:26 | ||||
| chr11:110088135-110088372 | Rare:31 | ||||
| chr11:110406329-110406697 | Common:3; Rare:65 | ||||
| chr11:114294959-114295095 | Rare:31 | ||||
| chr11:126409362-126409620 | Common:1; Rare:56 | ||||
| chr12:6602103-6602401 | Rare:94 | ||||
| chr12:6769598-6769973 | Common:1; Rare:105 |