| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:52455387-52455525 | Common:2; Rare:52 | ||||
| chr13:67230319-67230628 | Common:2; Rare:102 | ||||
| chr13:72727598-72727943 | Common:4; Rare:125 | ||||
| chr13:72781834-72782191 | Common:1; Rare:138 | ||||
| chr13:75635791-75635843 | Common:1; Rare:10 | ||||
| chr13:75635934-75635976 | Rare:8 | ||||
| chr13:75635997-75636405 | Common:2; Rare:101 | ||||
| chr13:93226798-93227134 | Common:1; Rare:69; Clinvar:1; Clinvar (benign):1 | ||||
| chr13:96053353-96053606 | Common:2; Rare:102 | ||||
| chr13:99200670-99200891 | Common:6; Rare:101 | ||||
| chr13:100088909-100089117 | Rare:76; Clinvar:1; Clinvar (benign):2 | ||||
| chr13:102596779-102597037 | Common:1; Rare:119 | ||||
| chr13:102798914-102799171 | Common:1; Rare:54 | ||||
| chr13:102845926-102846184 | Common:3; Rare:60; Clinvar:4; Clinvar (benign):1 | ||||
| chr13:106568098-106568278 | Rare:56 |