| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:11890622-11890897 | Common:2; Rare:99 | ||||
| chr20:13784884-13785080 | Common:2; Rare:87; Clinvar (benign):3 | ||||
| chr20:13995277-13995539 | Rare:64 | ||||
| chr20:16573297-16573540 | Common:1; Rare:68 | ||||
| chr20:16729922-16730073 | Rare:44 | ||||
| chr20:17558382-17558558 | Common:3; Rare:28 | ||||
| chr20:17558752-17558951 | Common:1; Rare:33 | ||||
| chr20:17569949-17570222 | Common:3; Rare:119 | ||||
| chr20:17968432-17968605 | Common:4; Rare:73 | ||||
| chr20:17968783-17969073 | Common:2; Rare:110 | ||||
| chr20:18467010-18467129 | Rare:32 | ||||
| chr20:18507430-18507595 | Rare:43; Clinvar:1 | ||||
| chr20:18507781-18507957 | Common:1; Rare:51; Clinvar:5; Clinvar (benign):1 | ||||
| chr20:21303179-21303417 | Rare:86 | ||||
| chr20:23350506-23350886 | Common:3; Rare:114 |