| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:58579970-58580400 | Common:8; Rare:151 | ||||
| chr11:58642203-58642603 | Common:4; Rare:122 | ||||
| chr11:58646950-58647560 | Common:9; Rare:170 | ||||
| chr11:58647490-58647780 | Common:4; Rare:66 | ||||
| chr11:59058480-59058860 | Common:2; Rare:194 | ||||
| chr11:59064260-59064780 | Common:6; Rare:186 | ||||
| chr11:59076699-59077522 | Rare:215 | ||||
| chr11:59097450-59097850 | Common:3; Rare:120 | ||||
| chr11:59097888-59098220 | Common:3; Rare:110 | ||||
| chr11:59102284-59102723 | Common:8; Rare:212 | ||||
| chr11:59105731-59106563 | Common:2; Rare:219 | ||||
| chr11:59107984-59108473 | Common:9; Rare:228 | ||||
| chr11:59151832-59152232 | Common:1; Rare:136; Clinvar (benign):1 | ||||
| chr11:59156521-59156921 | Common:4; Rare:108 | ||||
| chr11:59173213-59173315 | Common:1; Rare:12 |