| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:9115769-9115990 | Common:3; Rare:65 | ||||
| chr12:9116001-9116283 | Rare:50 | ||||
| chr12:9760898-9761112 | Rare:33 | ||||
| chr12:10212566-10212953 | Common:5; Rare:96 | ||||
| chr12:11171063-11171228 | Common:1; Rare:56 | ||||
| chr12:11171553-11171711 | Common:2; Rare:53 | ||||
| chr12:12356981-12357137 | Common:1; Rare:80 | ||||
| chr12:12562263-12562575 | Common:3; Rare:74 | ||||
| chr12:12717746-12717823 | Common:1; Rare:25; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:12891318-12891567 | Common:1; Rare:48 | ||||
| chr12:13000196-13000460 | Common:1; Rare:85 | ||||
| chr12:14365482-14365763 | Common:1; Rare:88 | ||||
| chr12:14774184-14774477 | Common:3; Rare:76 | ||||
| chr12:14803443-14803687 | Common:1; Rare:61 | ||||
| chr12:14948874-14949003 | Rare:19 |