| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:99980491-99980922 | Common:3; Rare:122 | ||||
| chr13:99980925-99980989 | Rare:19 | ||||
| chr13:99982840-99983153 | Common:1; Rare:52; Clinvar (benign):1 | ||||
| chr13:99983535-99983578 | Rare:8 | ||||
| chr13:99986007-99986053 | Rare:17 | ||||
| chr13:99986874-99986996 | Rare:19 | ||||
| chr13:99987030-99987132 | Rare:24 | ||||
| chr13:99987745-99987847 | Common:2; Rare:19 | ||||
| chr13:99987863-99987992 | Rare:28 | ||||
| chr13:99988993-99989474 | Common:3; Rare:91 | ||||
| chr13:99989663-99989752 | Rare:21 | ||||
| chr13:99990178-99990486 | Common:6; Rare:72 | ||||
| chr13:99990664-99990686 | Rare:4 | ||||
| chr13:99991464-99991671 | Common:1; Rare:40 | ||||
| chr13:99991736-99991783 | Rare:12 |