| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:3855551-3855729 | Common:2; Rare:36 | ||||
| chr11:4094603-4094907 | Common:2; Rare:85 | ||||
| chr11:4393651-4393820 | Rare:42 | ||||
| chr11:5226928-5227262 | Common:2; Rare:113; Clinvar:32; Clinvar (benign):4; Clinvar (pathogenic):36 | ||||
| chr11:5253270-5253533 | Common:3; Rare:68; Clinvar:3 | ||||
| chr11:5596610-5596714 | Common:3; Rare:36 | ||||
| chr11:5624882-5625033 | Rare:25 | ||||
| chr11:6390214-6390604 | Common:3; Rare:120; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:6431217-6431820 | Common:3; Rare:196 | ||||
| chr11:6440833-6441169 | Common:2; Rare:81 | ||||
| chr11:6481285-6481558 | Common:5; Rare:125 | ||||
| chr11:6603494-6603831 | Common:4; Rare:103; Clinvar (benign):3 | ||||
| chr11:7020303-7020524 | Rare:77 | ||||
| chr11:7513616-7514108 | Common:7; Rare:143 | ||||
| chr11:8682628-8683021 | Common:2; Rare:168 |