| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:94128631-94129810 | Common:27; Rare:1246 | ||||
| chr11:94493735-94494152 | Common:37; Rare:602; Clinvar:7; Clinvar (benign):14 | ||||
| chr11:94543660-94544500 | Common:21; Rare:873 | ||||
| chr11:94544568-94545168 | Common:8; Rare:490 | ||||
| chr11:94566761-94568060 | Common:14; Rare:681 | ||||
| chr11:94568108-94568535 | Rare:129 | ||||
| chr11:94767268-94768169 | Common:8; Rare:350 | ||||
| chr11:94768145-94768709 | Common:8; Rare:431 | ||||
| chr11:94768740-94769140 | Common:2; Rare:123 | ||||
| chr11:94973170-94973450 | Common:7; Rare:65 | ||||
| chr11:94973373-94973919 | Rare:594 | ||||
| chr11:95066903-95067910 | Common:12; Rare:1409 | ||||
| chr11:95089660-95090086 | Common:18; Rare:531 | ||||
| chr11:95231010-95231410 | Common:2; Rare:268 | ||||
| chr11:95231406-95231606 | Common:3; Rare:101 |