| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:2135833-2136144 | Common:1; Rare:151; Clinvar (benign):1 | ||||
| chr16:2136207-2136379 | Common:2; Rare:53 | ||||
| chr16:2148441-2148732 | Rare:102 | ||||
| chr16:2153248-2153464 | Common:1; Rare:113 | ||||
| chr16:2153488-2153877 | Common:4; Rare:144 | ||||
| chr16:2155222-2155909 | Common:2; Rare:234 | ||||
| chr16:2156051-2156150 | Rare:26 | ||||
| chr16:2205135-2205290 | Common:1; Rare:35 | ||||
| chr16:2205296-2205544 | Common:2; Rare:75 | ||||
| chr16:2205615-2205889 | Common:4; Rare:127 | ||||
| chr16:2206127-2206219 | Rare:24 | ||||
| chr16:2214335-2214452 | Rare:31 | ||||
| chr16:2214628-2214723 | Rare:23 | ||||
| chr16:2214742-2215196 | Common:3; Rare:175 | ||||
| chr16:2215200-2215488 | Common:1; Rare:78 |