| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:150428110-150428420 | Common:3; Rare:97 | ||||
| chr5:150542930-150543389 | Common:3; Rare:172; Clinvar (benign):1 | ||||
| chr5:150778658-150778764 | Common:1; Rare:42 | ||||
| chr5:151005301-151005854 | Common:6; Rare:137 | ||||
| chr5:151158431-151158637 | Common:2; Rare:73 | ||||
| chr5:151251140-151251448 | Common:2; Rare:58 | ||||
| chr5:154647040-154647630 | Common:3; Rare:197 | ||||
| chr5:154682320-154683056 | Common:8; Rare:217 | ||||
| chr5:157564513-157564614 | Rare:16 | ||||
| chr5:160467495-160468018 | Common:7; Rare:154 | ||||
| chr5:160477600-160478190 | Common:9; Rare:189 | ||||
| chr5:172772348-172772748 | Common:10; Rare:152 | ||||
| chr5:172778151-172778547 | Common:5; Rare:94 | ||||
| chr5:172807210-172807590 | Common:4; Rare:112 | ||||
| chr5:173294690-173294920 | Common:4; Rare:49 |