| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:49444010-49444477 | Common:1; Rare:151 | ||||
| chr13:49495902-49496223 | Common:3; Rare:78 | ||||
| chr13:49585520-49585658 | Common:1; Rare:50 | ||||
| chr13:49792507-49792752 | Common:5; Rare:104 | ||||
| chr13:49936176-49936586 | Common:1; Rare:130 | ||||
| chr13:49996739-49997107 | Common:1; Rare:79 | ||||
| chr13:50081921-50082296 | Common:1; Rare:101 | ||||
| chr13:50715471-50715697 | Rare:50 | ||||
| chr13:50909742-50910139 | Common:1; Rare:95; Clinvar:6; Clinvar (benign):1 | ||||
| chr13:51452244-51452383 | Rare:40 | ||||
| chr13:51452653-51452758 | Rare:23 | ||||
| chr13:51453013-51453388 | Rare:146 | ||||
| chr13:51804110-51804236 | Common:2; Rare:39 | ||||
| chr13:52011930-52012428 | Common:2; Rare:162; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr13:52406125-52406298 | Common:2; Rare:41 |