| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:20161484-20161816 | Common:2; Rare:86 | ||||
| chr13:20192299-20192547 | Rare:42 | ||||
| chr13:20192891-20193114 | Common:1; Rare:63; Clinvar:2; Clinvar (benign):2 | ||||
| chr13:20525777-20526003 | Common:2; Rare:80 | ||||
| chr13:20566708-20566900 | Rare:47 | ||||
| chr13:20566966-20567508 | Common:5; Rare:167 | ||||
| chr13:20704090-20704219 | Common:1; Rare:49 | ||||
| chr13:20773582-20773732 | Common:1; Rare:46 | ||||
| chr13:20773851-20774084 | Common:1; Rare:88 | ||||
| chr13:20902277-20902365 | Rare:14 | ||||
| chr13:20902665-20903143 | Common:2; Rare:150 | ||||
| chr13:21061510-21061784 | Common:1; Rare:79 | ||||
| chr13:21140120-21140684 | Common:1; Rare:200 | ||||
| chr13:21141015-21141219 | Common:1; Rare:42 | ||||
| chr13:21176205-21176402 | Common:4; Rare:57 |