| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:26222440-26222656 | Common:3; Rare:40 | ||||
| chr13:26253812-26254247 | Rare:125 | ||||
| chr13:26557438-26557781 | Common:4; Rare:137 | ||||
| chr13:26558107-26558560 | Common:16; Rare:203 | ||||
| chr13:27171037-27171267 | Common:3; Rare:56 | ||||
| chr13:27171757-27172178 | Common:1; Rare:146 | ||||
| chr13:27251224-27251630 | Common:8; Rare:129 | ||||
| chr13:27270660-27270832 | Common:1; Rare:56 | ||||
| chr13:27424230-27424780 | Common:5; Rare:155 | ||||
| chr13:27449968-27450283 | Common:3; Rare:101 | ||||
| chr13:27450560-27450714 | Rare:50 | ||||
| chr13:27620420-27620920 | Common:6; Rare:175 | ||||
| chr13:27621662-27621928 | Common:7; Rare:117; Clinvar:5; Clinvar (benign):5 | ||||
| chr13:28138071-28138243 | Common:2; Rare:56 | ||||
| chr13:28139266-28139609 | Common:1; Rare:79 |