| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:150137310-150137736 | Common:2; Rare:127 | ||||
| chr5:150357453-150357747 | Rare:99; Clinvar:2; Clinvar (benign):4 | ||||
| chr5:150412651-150413246 | Common:4; Rare:147 | ||||
| chr5:150446860-150447240 | Common:2; Rare:75 | ||||
| chr5:150449542-150449797 | Common:8; Rare:121 | ||||
| chr5:150485711-150485987 | Common:6; Rare:113 | ||||
| chr5:150486010-150486380 | Common:4; Rare:130 | ||||
| chr5:150486418-150486916 | Common:4; Rare:180 | ||||
| chr5:150700986-150701156 | Common:4; Rare:139 | ||||
| chr5:150758975-150759167 | Common:5; Rare:139 | ||||
| chr5:150904957-150905225 | Common:1; Rare:67 | ||||
| chr5:151020285-151020738 | Common:5; Rare:165 | ||||
| chr5:151080929-151081206 | Common:2; Rare:178 | ||||
| chr5:151157680-151157907 | Common:2; Rare:92 | ||||
| chr5:151211700-151212150 | Common:9; Rare:135 |