| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:95924084-95924164 | Rare:32 | ||||
| chr11:96389842-96390052 | Common:1; Rare:87 | ||||
| chr11:101583468-101583552 | Common:1; Rare:35; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:101914869-101915030 | Common:2; Rare:42 | ||||
| chr11:101915106-101915295 | Common:2; Rare:52 | ||||
| chr11:102047349-102047477 | Common:1; Rare:45 | ||||
| chr11:102347111-102347298 | Common:2; Rare:62 | ||||
| chr11:102452619-102452943 | Common:2; Rare:101 | ||||
| chr11:103109275-103109574 | Common:1; Rare:86; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:104164039-104164162 | Common:1; Rare:25 | ||||
| chr11:105610644-105610735 | Rare:20 | ||||
| chr11:106077326-106077711 | Common:2; Rare:115 | ||||
| chr11:108009254-108009349 | Rare:48 | ||||
| chr11:108222585-108222831 | Rare:89 | ||||
| chr11:108664789-108665110 | Common:5; Rare:121 |