| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:102799338-102800447 | Common:11; Rare:485 | ||||
| chr13:102845642-102846167 | Common:26; Rare:352; Clinvar:11; Clinvar (benign):12 | ||||
| chr13:102846502-102846902 | Common:3; Rare:132 | ||||
| chr13:106535540-106535726 | Common:2; Rare:91 | ||||
| chr13:106567020-106567530 | Common:4; Rare:125 | ||||
| chr13:106567872-106568286 | Rare:242 | ||||
| chr13:107865898-107866320 | Common:2; Rare:297 | ||||
| chr13:108215340-108215760 | Common:8; Rare:195 | ||||
| chr13:108218210-108218593 | Common:5; Rare:332 | ||||
| chr13:108218736-108219189 | Common:3; Rare:206 | ||||
| chr13:108779302-108779583 | Common:3; Rare:44 | ||||
| chr13:109786401-109787146 | Common:10; Rare:844 | ||||
| chr13:110507180-110507500 | Common:1; Rare:67 | ||||
| chr13:110561150-110561590 | Common:1; Rare:206 | ||||
| chr13:110561612-110562003 | Common:17; Rare:306 |