| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:110307838-110308152 | Common:1; Rare:114 | ||||
| chr13:110308524-110308622 | Common:1; Rare:15 | ||||
| chr13:110308977-110309231 | Common:3; Rare:47 | ||||
| chr13:110340888-110341209 | Common:3; Rare:73 | ||||
| chr13:110343297-110343374 | Rare:17 | ||||
| chr13:110388286-110388605 | Common:4; Rare:60 | ||||
| chr13:110416320-110416409 | Common:1; Rare:13 | ||||
| chr13:110424792-110424993 | Common:4; Rare:65; Clinvar:3; Clinvar (benign):2 | ||||
| chr13:110449512-110449793 | Common:4; Rare:75; Clinvar:1; Clinvar (benign):2 | ||||
| chr13:110503843-110504264 | Common:4; Rare:141; Clinvar:1; Clinvar (benign):4 | ||||
| chr14:24006983-24007116 | Common:1; Rare:41 | ||||
| chr14:32203267-32203564 | Common:12; Rare:124 | ||||
| chr14:34874103-34874215 | Common:1; Rare:32 | ||||
| chr14:35401955-35402289 | Common:5; Rare:99; Clinvar:1; Clinvar (benign):3 | ||||
| chr14:41605288-41605395 | Common:2; Rare:21 |