| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:89508272-89508403 | Common:1; Rare:74 | ||||
| chr16:89657621-89657825 | Common:1; Rare:101 | ||||
| chr16:89816622-89816760 | Common:2; Rare:65; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:89918708-89918872 | Common:4; Rare:50; Clinvar:2; Clinvar (benign):4 | ||||
| chr16:89921634-89921940 | Common:1; Rare:84 | ||||
| chr16:89972462-89972835 | Common:2; Rare:138 | ||||
| chr17:1491613-1491748 | Rare:41 | ||||
| chr17:1516566-1516934 | Common:1; Rare:129 | ||||
| chr17:1684799-1685042 | Common:2; Rare:79; Clinvar:4; Clinvar (benign):1 | ||||
| chr17:1716155-1716537 | Common:3; Rare:123 | ||||
| chr17:1829786-1830038 | Common:6; Rare:108 | ||||
| chr17:2303745-2303980 | Common:2; Rare:90 | ||||
| chr17:2336428-2336487 | Rare:21 | ||||
| chr17:2511845-2511971 | Common:2; Rare:34 | ||||
| chr17:2711742-2711818 | Rare:31 |