| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:151093531-151093734 | Common:1; Rare:35 | ||||
| chr5:151157691-151157914 | Common:2; Rare:92 | ||||
| chr5:151252720-151253400 | Common:7; Rare:264; Clinvar:2; Clinvar (benign):5 | ||||
| chr5:151758340-151759051 | Common:7; Rare:312 | ||||
| chr5:151771335-151772107 | Common:8; Rare:494 | ||||
| chr5:154038840-154039054 | Common:2; Rare:135 | ||||
| chr5:154190411-154190779 | Common:2; Rare:216 | ||||
| chr5:154445747-154446070 | Common:3; Rare:205 | ||||
| chr5:154754902-154755502 | Common:10; Rare:328 | ||||
| chr5:154793570-154794100 | Common:1; Rare:201 | ||||
| chr5:154858055-154858260 | Common:12; Rare:129 | ||||
| chr5:154858433-154858722 | Common:2; Rare:180 | ||||
| chr5:154938122-154938303 | Rare:122 | ||||
| chr5:154941001-154941259 | Common:2; Rare:182 | ||||
| chr5:157142660-157143301 | Common:12; Rare:297 |