| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:73059274-73059634 | Common:7; Rare:79 | ||||
| chr16:74296697-74296983 | Rare:112 | ||||
| chr16:74606964-74607147 | Rare:101 | ||||
| chr16:74666828-74667121 | Common:5; Rare:106 | ||||
| chr16:74774519-74774682 | Common:1; Rare:49; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):6 | ||||
| chr16:74999772-74999940 | Common:1; Rare:60 | ||||
| chr16:75250869-75250937 | Rare:25 | ||||
| chr16:75265841-75266031 | Common:3; Rare:78 | ||||
| chr16:75433291-75433454 | Rare:73 | ||||
| chr16:75433458-75433787 | Common:4; Rare:93 | ||||
| chr16:75623189-75623415 | Common:4; Rare:84 | ||||
| chr16:75636455-75636827 | Common:1; Rare:92; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr16:75647578-75647879 | Common:4; Rare:150; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr16:75648096-75648333 | Rare:93 | ||||
| chr16:75648447-75648550 | Rare:29 |