| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:535418-535792 | Common:10; Rare:244; Clinvar (benign):1 | ||||
| chr11:536775-537131 | Common:8; Rare:103 | ||||
| chr11:537230-537590 | Common:11; Rare:197 | ||||
| chr11:560703-561043 | Common:14; Rare:309 | ||||
| chr11:575826-576270 | Common:8; Rare:163 | ||||
| chr11:576412-576552 | Rare:93 | ||||
| chr11:615946-616191 | Common:1; Rare:78 | ||||
| chr11:695012-695388 | Common:2; Rare:185 | ||||
| chr11:695579-695979 | Common:5; Rare:156 | ||||
| chr11:706420-706660 | Common:1; Rare:69 | ||||
| chr11:706920-707220 | Common:3; Rare:90 | ||||
| chr11:747252-747569 | Rare:240; Clinvar:7; Clinvar (benign):2 | ||||
| chr11:777455-777663 | Common:4; Rare:173 | ||||
| chr11:797890-798120 | Common:4; Rare:139 | ||||
| chr11:805185-805480 | Common:12; Rare:202 |