| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:75482512-75482678 | Common:2; Rare:33 | ||||
| chr13:75537754-75538218 | Common:5; Rare:158 | ||||
| chr13:75549342-75549531 | Common:2; Rare:52 | ||||
| chr13:75549735-75549884 | Common:3; Rare:61 | ||||
| chr13:75549991-75550216 | Common:4; Rare:56 | ||||
| chr13:75635692-75636009 | Common:1; Rare:95 | ||||
| chr13:75636140-75636421 | Common:1; Rare:66 | ||||
| chr13:75636748-75636767 | Common:1; Rare:5 | ||||
| chr13:75636876-75637053 | Common:1; Rare:44 | ||||
| chr13:75760336-75760464 | Rare:28 | ||||
| chr13:75760505-75760974 | Common:3; Rare:139 | ||||
| chr13:76886374-76886668 | Common:2; Rare:91 | ||||
| chr13:76991869-76992844 | Common:12; Rare:280; Clinvar:25; Clinvar (benign):27; Clinvar (pathogenic):5 | ||||
| chr13:77026503-77026873 | Common:3; Rare:111 | ||||
| chr13:77027007-77027371 | Common:6; Rare:121 |