| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:95790359-95790585 | Common:1; Rare:88 | ||||
| chr11:95923789-95923863 | Common:1; Rare:22; Clinvar (benign):1 | ||||
| chr11:96389866-96390043 | Common:1; Rare:70 | ||||
| chr11:101583896-101584078 | Rare:49; Clinvar:1 | ||||
| chr11:101914869-101915069 | Common:3; Rare:56 | ||||
| chr11:101915108-101915310 | Common:3; Rare:58 | ||||
| chr11:102110124-102110454 | Rare:117 | ||||
| chr11:102347111-102347290 | Common:2; Rare:57 | ||||
| chr11:102452605-102452911 | Common:2; Rare:101 | ||||
| chr11:103092072-103092278 | Common:2; Rare:74 | ||||
| chr11:106077326-106077702 | Common:2; Rare:111 | ||||
| chr11:107457800-107457933 | Common:1; Rare:39 | ||||
| chr11:108009304-108009349 | Rare:23 | ||||
| chr11:108222594-108223050 | Rare:149; Clinvar:7 | ||||
| chr11:108467506-108467610 | Common:1; Rare:36 |