| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:75636872-75637029 | Common:1; Rare:38 | ||||
| chr13:75637077-75637353 | Common:2; Rare:60 | ||||
| chr13:76886278-76886668 | Common:4; Rare:140 | ||||
| chr13:76886846-76887124 | Common:3; Rare:50 | ||||
| chr13:76991906-76992435 | Common:6; Rare:199; Clinvar:25; Clinvar (benign):27; Clinvar (pathogenic):5 | ||||
| chr13:77026598-77026860 | Common:2; Rare:76 | ||||
| chr13:77027032-77027510 | Common:9; Rare:139 | ||||
| chr13:77326684-77326879 | Common:1; Rare:58 | ||||
| chr13:77326979-77327344 | Common:1; Rare:147 | ||||
| chr13:77697362-77697816 | Common:2; Rare:129 | ||||
| chr13:77697892-77698053 | Common:1; Rare:36 | ||||
| chr13:77698836-77699005 | Common:1; Rare:48 | ||||
| chr13:78603496-78603711 | Common:5; Rare:65 | ||||
| chr13:78658622-78658775 | Rare:42 | ||||
| chr13:78659084-78659258 | Common:2; Rare:115 |