| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:101583790-101584165 | Common:2; Rare:101; Clinvar:3; Clinvar (benign):3 | ||||
| chr11:101914869-101915073 | Common:4; Rare:58 | ||||
| chr11:101915105-101915376 | Common:3; Rare:81 | ||||
| chr11:102110201-102110471 | Common:1; Rare:105 | ||||
| chr11:102110920-102111164 | Rare:77; Clinvar:1 | ||||
| chr11:102347111-102347298 | Common:2; Rare:62 | ||||
| chr11:102452523-102452917 | Common:2; Rare:132 | ||||
| chr11:103092028-103092261 | Common:1; Rare:71 | ||||
| chr11:105034838-105035016 | Common:1; Rare:40 | ||||
| chr11:106077313-106077719 | Common:2; Rare:123 | ||||
| chr11:107457800-107457924 | Common:1; Rare:35 | ||||
| chr11:107565699-107565787 | Rare:26 | ||||
| chr11:108008998-108009237 | Rare:53 | ||||
| chr11:108009273-108009369 | Rare:43 | ||||
| chr11:108222585-108223122 | Common:1; Rare:171; Clinvar:7; Clinvar (benign):1 |