| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:120581353-120581577 | Common:1; Rare:78 | ||||
| chr12:121210056-121210152 | Common:2; Rare:33 | ||||
| chr12:121296697-121296923 | Common:1; Rare:67 | ||||
| chr12:121399895-121400154 | Common:5; Rare:93 | ||||
| chr12:121802913-121803091 | Rare:45 | ||||
| chr12:122526849-122527291 | Common:4; Rare:162 | ||||
| chr12:122752659-122752921 | Common:1; Rare:98 | ||||
| chr12:122980570-122980734 | Common:1; Rare:53 | ||||
| chr12:123233096-123233490 | Common:2; Rare:130; Clinvar:1 | ||||
| chr12:123272197-123272222 | Rare:6 | ||||
| chr12:123364820-123364948 | Common:1; Rare:49 | ||||
| chr12:123584314-123584609 | Common:6; Rare:98 | ||||
| chr12:123601832-123602139 | Common:6; Rare:78 | ||||
| chr12:123633607-123633851 | Common:1; Rare:117; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:123670991-123671216 | Common:4; Rare:57; Clinvar:1; Clinvar (benign):1 |