| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:108215527-108215789 | Common:1; Rare:67 | ||||
| chr13:108215826-108215838 | Rare:1 | ||||
| chr13:108218120-108218697 | Common:3; Rare:181 | ||||
| chr13:108269580-108269726 | Rare:20 | ||||
| chr13:108269817-108270394 | Common:1; Rare:156 | ||||
| chr13:109786535-109786842 | Common:1; Rare:105 | ||||
| chr13:110307154-110307312 | Common:1; Rare:56; Clinvar (benign):1 | ||||
| chr13:110561608-110562019 | Common:6; Rare:131 | ||||
| chr13:110615367-110615771 | Common:2; Rare:142 | ||||
| chr13:110706031-110706494 | Common:5; Rare:149; Clinvar:1; Clinvar (benign):7 | ||||
| chr13:110712131-110712522 | Common:1; Rare:129 | ||||
| chr13:110712830-110713345 | Common:2; Rare:238 | ||||
| chr13:110713481-110713759 | Common:2; Rare:105 | ||||
| chr13:110714897-110715082 | Common:1; Rare:55 | ||||
| chr13:110715134-110715582 | Common:3; Rare:167 |