| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:43151864-43151921 | Rare:12 | ||||
| chr22:43812228-43812448 | Common:4; Rare:73 | ||||
| chr22:43955303-43955562 | Common:3; Rare:79 | ||||
| chr22:44024189-44024414 | Common:1; Rare:74 | ||||
| chr22:44026233-44026332 | Rare:25 | ||||
| chr22:44068803-44069106 | Common:2; Rare:61 | ||||
| chr22:44181103-44181428 | Common:5; Rare:77 | ||||
| chr22:44498067-44498488 | Common:3; Rare:148 | ||||
| chr22:44668446-44668796 | Common:5; Rare:134 | ||||
| chr22:45163622-45164034 | Common:5; Rare:151 | ||||
| chr22:45671680-45672076 | Common:3; Rare:141 | ||||
| chr22:46053777-46053901 | Rare:44 | ||||
| chr22:46250254-46250408 | Common:2; Rare:47 | ||||
| chr22:46296745-46296918 | Rare:57 | ||||
| chr22:46335601-46335797 | Common:5; Rare:91; Clinvar:9; Clinvar (benign):9; Clinvar (pathogenic):1 |