| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:3855551-3855729 | Common:2; Rare:36 | ||||
| chr11:4094720-4094921 | Common:1; Rare:58 | ||||
| chr11:4393654-4393803 | Rare:35 | ||||
| chr11:5624925-5625033 | Rare:17 | ||||
| chr11:6390241-6390508 | Common:2; Rare:76 | ||||
| chr11:6481267-6481551 | Common:5; Rare:124 | ||||
| chr11:6603553-6603822 | Common:4; Rare:83; Clinvar (benign):3 | ||||
| chr11:7513632-7514003 | Common:6; Rare:113 | ||||
| chr11:7673441-7673575 | Common:1; Rare:45 | ||||
| chr11:7965439-7965761 | Common:1; Rare:46 | ||||
| chr11:8682628-8682816 | Common:2; Rare:85 | ||||
| chr11:8964366-8964523 | Common:4; Rare:52 | ||||
| chr11:9460650-9461073 | Common:4; Rare:107 | ||||
| chr11:9663882-9664278 | Common:4; Rare:133 | ||||
| chr11:10304767-10305157 | Common:1; Rare:90 |