| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:85011292-85011655 | Common:9; Rare:147 | ||||
| chr16:85027602-85027788 | Common:1; Rare:98 | ||||
| chr16:85613206-85613345 | Rare:48 | ||||
| chr16:85799535-85799760 | Common:2; Rare:66 | ||||
| chr16:86555182-86555320 | Rare:71 | ||||
| chr16:87383734-87383976 | Common:1; Rare:102 | ||||
| chr16:87765949-87766055 | Common:1; Rare:39 | ||||
| chr16:88570166-88570467 | Common:2; Rare:113 | ||||
| chr16:88663084-88663377 | Common:8; Rare:121 | ||||
| chr16:88686487-88686789 | Common:3; Rare:92 | ||||
| chr16:88706343-88706525 | Common:3; Rare:87 | ||||
| chr16:88785218-88785435 | Common:1; Rare:66 | ||||
| chr16:88785515-88785711 | Rare:45 | ||||
| chr16:88803578-88803814 | Common:5; Rare:104 | ||||
| chr16:88856918-88857153 | Common:4; Rare:107; Clinvar:1; Clinvar (benign):2 |