| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:95923829-95923863 | Common:1; Rare:12; Clinvar (benign):1 | ||||
| chr11:96389854-96390044 | Common:1; Rare:78 | ||||
| chr11:101915108-101915249 | Rare:32 | ||||
| chr11:102110201-102110454 | Rare:99 | ||||
| chr11:102317254-102317532 | Rare:58 | ||||
| chr11:102347105-102347317 | Common:2; Rare:69 | ||||
| chr11:102452546-102452949 | Common:2; Rare:130 | ||||
| chr11:103092028-103092262 | Common:1; Rare:72 | ||||
| chr11:103109336-103109577 | Common:1; Rare:70; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:106077317-106077711 | Common:2; Rare:119 | ||||
| chr11:107457806-107457950 | Common:2; Rare:43 | ||||
| chr11:108008820-108008977 | Rare:46 | ||||
| chr11:108009312-108009351 | Rare:21 | ||||
| chr11:108222603-108223050 | Rare:144; Clinvar:7 | ||||
| chr11:108467469-108467618 | Common:3; Rare:59 |