| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:73058985-73059321 | Common:1; Rare:50 | ||||
| chr16:74296450-74296890 | Common:2; Rare:271 | ||||
| chr16:74607068-74607211 | Rare:140 | ||||
| chr16:74666771-74667209 | Common:16; Rare:283 | ||||
| chr16:74700614-74701219 | Common:7; Rare:190 | ||||
| chr16:74741013-74741220 | Common:2; Rare:78 | ||||
| chr16:74774579-74775003 | Common:10; Rare:245; Clinvar:9; Clinvar (benign):4; Clinvar (pathogenic):5 | ||||
| chr16:74984998-74985343 | Common:4; Rare:208 | ||||
| chr16:74998742-74999071 | Common:3; Rare:117 | ||||
| chr16:75148361-75148567 | Common:4; Rare:89 | ||||
| chr16:75148493-75149114 | Common:8; Rare:390 | ||||
| chr16:75265927-75266084 | Common:7; Rare:132 | ||||
| chr16:75266130-75266480 | Common:7; Rare:170 | ||||
| chr16:75433356-75433871 | Common:8; Rare:285 | ||||
| chr16:75464361-75464470 | Common:2; Rare:55 |