| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:104207979-104208112 | Common:2; Rare:54 | ||||
| chr7:105013581-105013719 | Common:1; Rare:46 | ||||
| chr7:105014097-105014261 | Common:1; Rare:68 | ||||
| chr7:105532071-105532231 | Rare:43 | ||||
| chr7:105876477-105876818 | Common:6; Rare:100 | ||||
| chr7:106112477-106112711 | Common:1; Rare:95 | ||||
| chr7:106284885-106285262 | Common:2; Rare:152 | ||||
| chr7:106285539-106285545 | |||||
| chr7:107563888-107563996 | Common:2; Rare:64; Clinvar (benign):2 | ||||
| chr7:107580144-107580294 | Common:2; Rare:61 | ||||
| chr7:107744053-107744190 | Rare:46 | ||||
| chr7:108526099-108526416 | Common:5; Rare:104 | ||||
| chr7:108569592-108570013 | Common:2; Rare:149 | ||||
| chr7:111090847-111091142 | Rare:52 | ||||
| chr7:112206317-112206805 | Common:2; Rare:173 |