| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:52159558-52159623 | Common:1; Rare:13 | ||||
| chr13:52455208-52455576 | Common:3; Rare:127 | ||||
| chr13:52455926-52456027 | Common:1; Rare:33 | ||||
| chr13:52652281-52652413 | Common:3; Rare:37 | ||||
| chr13:52652652-52652958 | Common:3; Rare:102 | ||||
| chr13:52653086-52653164 | Rare:29 | ||||
| chr13:60163875-60164119 | Common:1; Rare:63 | ||||
| chr13:60397161-60397380 | Common:4; Rare:80 | ||||
| chr13:67230287-67230453 | Common:1; Rare:48 | ||||
| chr13:72727579-72727972 | Common:6; Rare:150 | ||||
| chr13:72781852-72782273 | Common:1; Rare:150 | ||||
| chr13:75482392-75482488 | Common:1; Rare:24 | ||||
| chr13:75549353-75549831 | Common:9; Rare:128 | ||||
| chr13:75550061-75550146 | Common:1; Rare:23 | ||||
| chr13:76992038-76992214 | Common:1; Rare:81; Clinvar:10; Clinvar (benign):9; Clinvar (pathogenic):3 |