| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:13919918-13920199 | Common:3; Rare:108; Clinvar:3; Clinvar (benign):1 | ||||
| chr16:14071024-14071360 | Common:3; Rare:116 | ||||
| chr16:14630188-14630395 | Rare:93 | ||||
| chr16:14632729-14632999 | Common:1; Rare:90 | ||||
| chr16:14975052-14975191 | Rare:23 | ||||
| chr16:15094229-15094409 | Common:1; Rare:90 | ||||
| chr16:15643022-15643267 | Rare:74 | ||||
| chr16:15650087-15650289 | Common:1; Rare:103 | ||||
| chr16:15857015-15857287 | Common:5; Rare:65; Clinvar (benign):1 | ||||
| chr16:18925751-18925904 | Common:2; Rare:52 | ||||
| chr16:18926372-18926588 | Common:1; Rare:95 | ||||
| chr16:19067415-19067699 | Common:5; Rare:116; Clinvar:1 | ||||
| chr16:19067773-19067920 | Common:2; Rare:35 | ||||
| chr16:19411040-19411078 | Rare:6 | ||||
| chr16:19417764-19417981 | Common:3; Rare:35 |