| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:107797084-107797367 | Common:4; Rare:57 | ||||
| chr13:107867432-107867715 | Common:5; Rare:93 | ||||
| chr13:110151336-110151567 | Common:2; Rare:41 | ||||
| chr13:110178929-110179334 | Common:4; Rare:109; Clinvar:2; Clinvar (benign):1 | ||||
| chr13:110213461-110213706 | Common:3; Rare:43 | ||||
| chr13:110297952-110298207 | Common:1; Rare:43 | ||||
| chr13:110308524-110308604 | Common:1; Rare:13 | ||||
| chr13:110327042-110327316 | Common:2; Rare:56 | ||||
| chr13:110403315-110403604 | Common:4; Rare:39 | ||||
| chr13:110406309-110406565 | Common:2; Rare:47 | ||||
| chr13:110439577-110439786 | Common:1; Rare:33 | ||||
| chr13:110476366-110476767 | Common:4; Rare:97 | ||||
| chr13:110503900-110504289 | Common:4; Rare:131; Clinvar:1; Clinvar (benign):3 | ||||
| chr13:110870226-110870560 | Common:3; Rare:51 | ||||
| chr13:110896992-110897317 | Common:4; Rare:79 |