| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:178232540-178232893 | Common:4; Rare:117 | ||||
| chr5:179618035-179618182 | Common:1; Rare:59 | ||||
| chr5:180810121-180810284 | Common:5; Rare:49 | ||||
| chr5:181261081-181261274 | Rare:66 | ||||
| chr6:693054-693212 | Rare:49 | ||||
| chr6:2245585-2245776 | Rare:61 | ||||
| chr6:3456063-3456181 | Rare:40 | ||||
| chr6:5003603-5003843 | Common:6; Rare:76 | ||||
| chr6:5260696-5261068 | Common:6; Rare:129; Clinvar (benign):4 | ||||
| chr6:5261260-5261585 | Common:9; Rare:90 | ||||
| chr6:7910775-7910893 | Common:1; Rare:42 | ||||
| chr6:8435412-8435620 | Common:3; Rare:72 | ||||
| chr6:10694622-10694995 | Common:4; Rare:95 | ||||
| chr6:11094107-11094274 | Rare:52 | ||||
| chr6:13615170-13615505 | Common:2; Rare:139 |