| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:116772938-116773160 | Common:1; Rare:135 | ||||
| chr11:116787988-116788097 | Rare:33 | ||||
| chr11:116791250-116791740 | Common:4; Rare:131; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:116792385-116792580 | Common:1; Rare:38 | ||||
| chr11:116823230-116823820 | Common:7; Rare:177 | ||||
| chr11:116829065-116829360 | Common:8; Rare:99 | ||||
| chr11:116829662-116829928 | Rare:118 | ||||
| chr11:116837449-116837896 | Common:3; Rare:88 | ||||
| chr11:117098270-117098626 | Common:1; Rare:183 | ||||
| chr11:117144173-117144374 | Common:4; Rare:191 | ||||
| chr11:117144553-117145070 | Common:15; Rare:266 | ||||
| chr11:117178631-117178816 | Common:1; Rare:65 | ||||
| chr11:117199047-117199375 | Common:11; Rare:189 | ||||
| chr11:117232036-117232180 | Rare:70 | ||||
| chr11:117232493-117232750 | Common:4; Rare:158 |