| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:112588104-112588229 | Rare:61 | ||||
| chr13:112689733-112690348 | Common:11; Rare:319 | ||||
| chr13:112893895-112894600 | Common:27; Rare:316 | ||||
| chr13:112969071-112969367 | Common:4; Rare:125 | ||||
| chr13:112984750-112985470 | Common:16; Rare:184 | ||||
| chr13:113105341-113106001 | Common:11; Rare:244; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):3 | ||||
| chr13:113122619-113122918 | Common:5; Rare:146; Clinvar:4; Clinvar (benign):2 | ||||
| chr13:113158436-113158658 | Common:4; Rare:98 | ||||
| chr13:113158850-113159190 | Common:4; Rare:116 | ||||
| chr13:113208583-113208787 | Rare:215 | ||||
| chr13:113208960-113209126 | Common:6; Rare:114 | ||||
| chr13:113209455-113209687 | Common:6; Rare:130 | ||||
| chr13:113297016-113297382 | Common:3; Rare:241 | ||||
| chr13:113364008-113364485 | Common:6; Rare:119 | ||||
| chr13:113449088-113449415 | Common:2; Rare:149 |