| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:103956907-103957234 | Common:4; Rare:69 | ||||
| chr12:103965664-103966056 | Common:4; Rare:108 | ||||
| chr12:104064457-104064559 | Rare:28 | ||||
| chr12:104138089-104138376 | Common:1; Rare:69 | ||||
| chr12:104286963-104287359 | Common:3; Rare:91 | ||||
| chr12:105107641-105107852 | Common:1; Rare:93; Clinvar:1 | ||||
| chr12:105236065-105236277 | Common:2; Rare:95 | ||||
| chr12:106247619-106247650 | Rare:9 | ||||
| chr12:106247910-106248074 | Common:1; Rare:47 | ||||
| chr12:106357441-106357823 | Common:4; Rare:65; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:106358010-106358112 | Common:3; Rare:34 | ||||
| chr12:106955647-106956014 | Common:2; Rare:129 | ||||
| chr12:106987007-106987131 | Common:2; Rare:34 | ||||
| chr12:107093537-107093666 | Rare:42 | ||||
| chr12:107318339-107318428 | Common:1; Rare:16 |