| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:104064442-104064624 | Rare:50 | ||||
| chr12:104138132-104138411 | Common:1; Rare:73 | ||||
| chr12:104216098-104216222 | Rare:30 | ||||
| chr12:104286761-104287153 | Common:3; Rare:71 | ||||
| chr12:104287173-104287430 | Rare:64 | ||||
| chr12:104288744-104289040 | Common:1; Rare:116 | ||||
| chr12:104958237-104958464 | Common:4; Rare:67 | ||||
| chr12:104986184-104986390 | Common:5; Rare:78 | ||||
| chr12:105107609-105107806 | Common:1; Rare:93; Clinvar:1 | ||||
| chr12:105236021-105236286 | Common:2; Rare:111 | ||||
| chr12:106302917-106303078 | Common:3; Rare:24 | ||||
| chr12:106357687-106357823 | Common:3; Rare:32; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:106357988-106358100 | Common:3; Rare:45 | ||||
| chr12:106774107-106774381 | Common:3; Rare:71 | ||||
| chr12:106955616-106955912 | Rare:110 |