| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:123458080-123458230 | Common:2; Rare:69 | ||||
| chr12:123533614-123533772 | Common:1; Rare:57 | ||||
| chr12:123533870-123534270 | Common:5; Rare:141 | ||||
| chr12:123584278-123584809 | Common:16; Rare:316 | ||||
| chr12:123601790-123602242 | Common:9; Rare:188 | ||||
| chr12:123633563-123633907 | Common:4; Rare:293; Clinvar:16; Clinvar (benign):2 | ||||
| chr12:123671016-123671211 | Common:4; Rare:51; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:123712182-123712425 | Common:8; Rare:185; Clinvar:4; Clinvar (benign):4 | ||||
| chr12:123972829-123973355 | Common:4; Rare:332 | ||||
| chr12:124422430-124423350 | Common:16; Rare:412 | ||||
| chr12:124567545-124567778 | Common:5; Rare:126 | ||||
| chr12:124863659-124864049 | Common:5; Rare:177 | ||||
| chr12:124913947-124914347 | Common:15; Rare:205 | ||||
| chr12:124914538-124915099 | Common:17; Rare:364 | ||||
| chr12:124917170-124917700 | Common:4; Rare:249 |