| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:173369802-173369935 | Common:1; Rare:45 | ||||
| chr4:174283584-174283965 | Common:1; Rare:73 | ||||
| chr4:174522359-174522613 | Rare:81; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr4:176195544-176195685 | Common:1; Rare:53 | ||||
| chr4:176319738-176320036 | Common:3; Rare:103 | ||||
| chr4:177442376-177442514 | Rare:83; Clinvar:2 | ||||
| chr4:183504529-183504792 | Common:1; Rare:88 | ||||
| chr4:183659105-183659354 | Common:1; Rare:85 | ||||
| chr4:184474517-184474811 | Rare:65 | ||||
| chr4:184649427-184649783 | Common:4; Rare:116 | ||||
| chr4:185396581-185396851 | Rare:86 | ||||
| chr4:185425866-185426278 | Common:4; Rare:126 | ||||
| chr4:189940613-189940991 | Common:11; Rare:134 | ||||
| chr5:218117-218361 | Common:3; Rare:99; Clinvar:5; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr5:612211-612346 | Rare:51 |