| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:50909684-50910123 | Common:1; Rare:101; Clinvar:6; Clinvar (benign):1 | ||||
| chr13:51453025-51453363 | Rare:124 | ||||
| chr13:51584203-51584492 | Common:3; Rare:95 | ||||
| chr13:51804136-51804255 | Common:2; Rare:35 | ||||
| chr13:52159558-52159719 | Common:1; Rare:26 | ||||
| chr13:52455229-52455543 | Common:3; Rare:107 | ||||
| chr13:52652666-52652916 | Common:3; Rare:80 | ||||
| chr13:52652952-52653154 | Rare:79 | ||||
| chr13:60163877-60164118 | Common:1; Rare:63 | ||||
| chr13:60397162-60397356 | Common:4; Rare:74 | ||||
| chr13:72727559-72727972 | Common:7; Rare:162 | ||||
| chr13:72781876-72782227 | Common:1; Rare:128 | ||||
| chr13:75537807-75538120 | Common:3; Rare:92 | ||||
| chr13:75549363-75549823 | Common:9; Rare:122 | ||||
| chr13:76991988-76992194 | Common:3; Rare:98; Clinvar:16; Clinvar (benign):12; Clinvar (pathogenic):3 |