| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:89217619-89217759 | Common:1; Rare:67 | ||||
| chr16:89490532-89490937 | Common:6; Rare:140 | ||||
| chr16:89508251-89508594 | Common:3; Rare:173; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr16:89560537-89560811 | Rare:115 | ||||
| chr16:89562821-89562936 | Rare:50 | ||||
| chr16:89593894-89594246 | Common:7; Rare:93 | ||||
| chr16:89657586-89658161 | Common:5; Rare:281; Clinvar (benign):1 | ||||
| chr16:89686601-89686736 | Common:8; Rare:74 | ||||
| chr16:89686919-89687018 | Rare:45 | ||||
| chr16:89701631-89701844 | Common:1; Rare:80 | ||||
| chr16:89711834-89711941 | Rare:56 | ||||
| chr16:89720862-89721016 | Common:1; Rare:47 | ||||
| chr16:89721281-89721583 | Common:3; Rare:125 | ||||
| chr16:89816611-89816754 | Common:1; Rare:70; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr16:89873508-89873856 | Common:3; Rare:152 |