| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:80341078-80342046 | Common:7; Rare:655 | ||||
| chr13:91398420-91398860 | Common:8; Rare:341 | ||||
| chr13:93226417-93227283 | Common:15; Rare:472; Clinvar:2; Clinvar (benign):6 | ||||
| chr13:94595562-94595962 | Rare:88 | ||||
| chr13:94596068-94596468 | Common:12; Rare:537 | ||||
| chr13:94601468-94601941 | Common:25; Rare:692 | ||||
| chr13:94601921-94602321 | Common:4; Rare:210 | ||||
| chr13:95301280-95302328 | Common:14; Rare:840 | ||||
| chr13:95676740-95677242 | Common:25; Rare:920 | ||||
| chr13:96053242-96053642 | Common:15; Rare:645 | ||||
| chr13:97222053-97223313 | Common:3; Rare:413 | ||||
| chr13:97433450-97435238 | Common:12; Rare:1400 | ||||
| chr13:97975540-97976119 | Common:8; Rare:264 | ||||
| chr13:97976038-97976735 | Common:11; Rare:1034 | ||||
| chr13:97976972-97977970 | Common:9; Rare:368 |