| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:88990603-88991604 | Common:16; Rare:356; Clinvar:1; Clinvar (benign):2 | ||||
| chr10:89301870-89302550 | Common:5; Rare:247 | ||||
| chr10:89327454-89328640 | Common:27; Rare:571 | ||||
| chr10:89332264-89333246 | Common:18; Rare:314 | ||||
| chr10:89392300-89392740 | Common:21; Rare:272 | ||||
| chr10:89414314-89414750 | Common:9; Rare:162 | ||||
| chr10:89643812-89644231 | Common:1; Rare:372 | ||||
| chr10:89644260-89644570 | Common:1; Rare:93 | ||||
| chr10:89644680-89646219 | Common:31; Rare:1471 | ||||
| chr10:89701311-89701711 | Common:18; Rare:644 | ||||
| chr10:89701720-89702000 | Rare:116 | ||||
| chr10:90857285-90858282 | Common:8; Rare:576 | ||||
| chr10:90871238-90871645 | Common:2; Rare:154 | ||||
| chr10:90871738-90872138 | Common:13; Rare:289 | ||||
| chr10:91162758-91163410 | Common:8; Rare:551 |