| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:94601600-94601918 | Common:3; Rare:92 | ||||
| chr13:95301399-95301667 | Rare:68 | ||||
| chr13:95676819-95677200 | Common:4; Rare:151 | ||||
| chr13:96053327-96053526 | Common:2; Rare:94 | ||||
| chr13:98977857-98978183 | Common:2; Rare:75 | ||||
| chr13:99200666-99200909 | Common:6; Rare:117 | ||||
| chr13:99307354-99307706 | Common:3; Rare:52 | ||||
| chr13:99606507-99606718 | Common:5; Rare:69 | ||||
| chr13:100088859-100089139 | Rare:108; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr13:100674778-100675137 | Common:4; Rare:149 | ||||
| chr13:102596773-102597102 | Common:1; Rare:134; Clinvar (benign):1 | ||||
| chr13:102773716-102773842 | Rare:59 | ||||
| chr13:102798955-102799191 | Common:1; Rare:49 | ||||
| chr13:102845689-102846157 | Common:9; Rare:124; Clinvar:4; Clinvar (benign):4 | ||||
| chr13:106567577-106567737 | Rare:52 |