| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:112996769-112997064 | Common:4; Rare:65 | ||||
| chr13:113234915-113235107 | Common:1; Rare:44 | ||||
| chr13:113334820-113334897 | Common:1; Rare:21 | ||||
| chr13:113859863-113859952 | Common:2; Rare:10 | ||||
| chr14:20456515-20456705 | Common:1; Rare:52; Clinvar:1 | ||||
| chr14:22770904-22771129 | Common:1; Rare:77 | ||||
| chr14:22773668-22773871 | Common:1; Rare:60; Clinvar (pathogenic):1 | ||||
| chr14:22821370-22821621 | Common:1; Rare:39 | ||||
| chr14:24036330-24036470 | Common:2; Rare:55 | ||||
| chr14:24072473-24072739 | Common:1; Rare:58 | ||||
| chr14:25048301-25048455 | Rare:25 | ||||
| chr14:31944526-31944838 | Common:3; Rare:59 | ||||
| chr14:32203267-32203650 | Common:13; Rare:163 | ||||
| chr14:34038725-34038936 | Rare:37 | ||||
| chr14:34874137-34874231 | Common:1; Rare:26 |