| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:110122854-110123316 | Common:4; Rare:142 | ||||
| chr13:110128044-110128226 | Common:1; Rare:30 | ||||
| chr13:110132690-110132990 | Common:5; Rare:53 | ||||
| chr13:110137048-110137448 | Common:5; Rare:144 | ||||
| chr13:110137942-110138380 | Common:2; Rare:87 | ||||
| chr13:110138390-110138810 | Common:3; Rare:162 | ||||
| chr13:110340880-110341160 | Common:3; Rare:62 | ||||
| chr13:110372034-110372190 | Rare:28 | ||||
| chr13:110443730-110444160 | Common:1; Rare:95 | ||||
| chr13:110446931-110447331 | Common:8; Rare:102 | ||||
| chr13:110471170-110471600 | Common:10; Rare:136 | ||||
| chr13:110471810-110472180 | Common:10; Rare:131 | ||||
| chr13:110475630-110476010 | Common:2; Rare:71 | ||||
| chr13:110503470-110503970 | Common:11; Rare:199; Clinvar (benign):5 | ||||
| chr13:110510172-110510572 | Common:2; Rare:102 |