| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:14953482-14954323 | Common:7; Rare:674; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr10:14954330-14954610 | Common:8; Rare:179 | ||||
| chr10:14959090-14960140 | Common:28; Rare:1290 | ||||
| chr10:15088644-15089044 | Common:5; Rare:302 | ||||
| chr10:15096865-15097265 | Common:16; Rare:413 | ||||
| chr10:15097292-15097447 | Common:5; Rare:275 | ||||
| chr10:15097440-15098301 | Common:15; Rare:320 | ||||
| chr10:15167961-15169833 | Common:49; Rare:1544 | ||||
| chr10:15370367-15371560 | Common:18; Rare:582 | ||||
| chr10:15603500-15603995 | Common:11; Rare:192 | ||||
| chr10:15859578-15860250 | Common:6; Rare:171 | ||||
| chr10:15860280-15860720 | Common:4; Rare:390 | ||||
| chr10:16436679-16437104 | Common:6; Rare:267 | ||||
| chr10:16437360-16437650 | Rare:75 | ||||
| chr10:16817151-16817975 | Common:32; Rare:1241 |