| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:142302393-142302580 | Common:1; Rare:45 | ||||
| chr6:143060724-143060925 | Common:7; Rare:70 | ||||
| chr6:143450660-143450929 | Common:1; Rare:101; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:143511662-143511932 | Common:4; Rare:56 | ||||
| chr6:145814718-145814939 | Common:1; Rare:103 | ||||
| chr6:149749662-149749796 | Rare:77 | ||||
| chr6:151325409-151325699 | Common:2; Rare:66 | ||||
| chr6:151391509-151391842 | Common:3; Rare:92 | ||||
| chr6:151452032-151452548 | Common:4; Rare:182 | ||||
| chr6:152983021-152983262 | Common:2; Rare:75 | ||||
| chr6:153002685-153002838 | Common:2; Rare:47 | ||||
| chr6:155314447-155314774 | Common:10; Rare:119 | ||||
| chr6:158168219-158168388 | Common:2; Rare:61 | ||||
| chr6:158644704-158645035 | Common:2; Rare:110 | ||||
| chr6:158649883-158650051 | Rare:34 |