| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:9575486-9575554 | Common:1; Rare:9 | ||||
| chr11:9663995-9664157 | Common:4; Rare:55 | ||||
| chr11:10304866-10305078 | Common:1; Rare:46 | ||||
| chr11:10541145-10541345 | Rare:74 | ||||
| chr11:10751174-10751302 | Rare:39 | ||||
| chr11:10808894-10809088 | Rare:78 | ||||
| chr11:10858019-10858266 | Common:3; Rare:81 | ||||
| chr11:11841903-11842077 | Common:1; Rare:50 | ||||
| chr11:14499782-14499913 | Common:2; Rare:47 | ||||
| chr11:14520318-14520484 | Rare:47 | ||||
| chr11:16738466-16738687 | Common:2; Rare:44 | ||||
| chr11:17077608-17077854 | Common:2; Rare:102 | ||||
| chr11:17207920-17208111 | Common:1; Rare:72 | ||||
| chr11:17719283-17719573 | Common:5; Rare:65 | ||||
| chr11:18322131-18322312 | Common:3; Rare:61; Clinvar:1; Clinvar (benign):2 |