| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:26937932-26938038 | Common:3; Rare:30 | ||||
| chr12:26938263-26938552 | Common:3; Rare:109 | ||||
| chr12:27244064-27244328 | Common:2; Rare:84 | ||||
| chr12:27523990-27524282 | Rare:67 | ||||
| chr12:27710709-27710853 | Common:1; Rare:53 | ||||
| chr12:28190371-28190502 | Common:1; Rare:42 | ||||
| chr12:29381140-29381334 | Common:2; Rare:59 | ||||
| chr12:30695860-30696002 | Common:1; Rare:32 | ||||
| chr12:30754749-30755051 | Common:1; Rare:119 | ||||
| chr12:31073769-31073902 | Common:1; Rare:52 | ||||
| chr12:31326111-31326457 | Common:4; Rare:120 | ||||
| chr12:31729005-31729267 | Rare:76 | ||||
| chr12:31959250-31959488 | Common:2; Rare:78 | ||||
| chr12:32679107-32679358 | Common:1; Rare:103; Clinvar:1; Clinvar (benign):4 | ||||
| chr12:42326009-42326215 | Common:1; Rare:66 |