| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:152269533-152269754 | Common:2; Rare:61 | ||||
| chr3:152298680-152299050 | Rare:66 | ||||
| chr3:154324419-154324573 | Rare:59 | ||||
| chr3:155079836-155080282 | Common:1; Rare:98 | ||||
| chr3:155854364-155854804 | Rare:127 | ||||
| chr3:155870323-155870727 | Common:2; Rare:118 | ||||
| chr3:156554992-156555334 | Common:1; Rare:138 | ||||
| chr3:156674362-156674631 | Common:3; Rare:79 | ||||
| chr3:157160090-157160327 | Rare:100 | ||||
| chr3:157533554-157533816 | Common:5; Rare:42 | ||||
| chr3:157543220-157543400 | Rare:43 | ||||
| chr3:158105739-158105902 | Common:5; Rare:82; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:158109836-158110162 | Rare:72 | ||||
| chr3:158672329-158672759 | Common:6; Rare:134 | ||||
| chr3:158732141-158732390 | Common:10; Rare:74 |