| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:70077981-70078690 | Common:7; Rare:291 | ||||
| chr11:70203092-70203394 | Common:4; Rare:113 | ||||
| chr11:70270413-70270764 | Common:2; Rare:141 | ||||
| chr11:70398313-70398593 | Common:3; Rare:98 | ||||
| chr11:71252484-71252912 | Common:4; Rare:105 | ||||
| chr11:71448342-71448549 | Common:2; Rare:64; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:71786730-71787190 | Common:5; Rare:129 | ||||
| chr11:71787307-71787585 | Common:15; Rare:114 | ||||
| chr11:71928189-71928320 | Rare:29 | ||||
| chr11:71928398-71928701 | Rare:81 | ||||
| chr11:71928930-71929114 | Common:1; Rare:62 | ||||
| chr11:72040762-72040913 | Rare:29 | ||||
| chr11:72041098-72041414 | Common:1; Rare:52 | ||||
| chr11:72041680-72041947 | Common:2; Rare:56 | ||||
| chr11:72070062-72070176 | Rare:12 |