| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:122980552-122980956 | Common:2; Rare:116 | ||||
| chr12:122981875-122982074 | Rare:70 | ||||
| chr12:123233087-123233490 | Common:2; Rare:134; Clinvar:1 | ||||
| chr12:123364735-123364989 | Common:5; Rare:113 | ||||
| chr12:123383706-123383953 | Rare:58 | ||||
| chr12:123383986-123384188 | Rare:54 | ||||
| chr12:123389866-123390033 | Rare:46 | ||||
| chr12:123390090-123390318 | Rare:68 | ||||
| chr12:123436152-123436229 | Rare:18 | ||||
| chr12:123436231-123436563 | Common:1; Rare:97 | ||||
| chr12:123436622-123436979 | Common:2; Rare:72 | ||||
| chr12:123533259-123533337 | Common:1; Rare:18 | ||||
| chr12:123584307-123584813 | Common:9; Rare:170 | ||||
| chr12:123602023-123602178 | Common:3; Rare:57 | ||||
| chr12:123633597-123633856 | Common:1; Rare:126; Clinvar:8; Clinvar (benign):1 |