| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:46846140-46846480 | Common:1; Rare:107 | ||||
| chr11:46918530-46918680 | Common:2; Rare:33; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:46936610-46937019 | Common:2; Rare:107 | ||||
| chr11:47176297-47176493 | Rare:46 | ||||
| chr11:47176770-47177176 | Common:1; Rare:173 | ||||
| chr11:47177357-47177388 | Rare:3 | ||||
| chr11:47185366-47185592 | Common:2; Rare:47 | ||||
| chr11:47185604-47185961 | Common:1; Rare:67 | ||||
| chr11:47186327-47186608 | Rare:70 | ||||
| chr11:47214281-47214554 | Common:1; Rare:30 | ||||
| chr11:47214779-47215528 | Common:2; Rare:192; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:47248566-47249189 | Common:2; Rare:171; Clinvar (benign):1 | ||||
| chr11:47257486-47257642 | Common:1; Rare:28 | ||||
| chr11:47257769-47257978 | Rare:39 | ||||
| chr11:47257998-47258069 | Rare:9 |