| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:179550528-179550858 | Common:2; Rare:150 | ||||
| chr5:179623602-179623994 | Common:4; Rare:141 | ||||
| chr5:179698667-179699091 | Common:4; Rare:138 | ||||
| chr5:179806310-179806448 | Rare:43 | ||||
| chr5:179806900-179807066 | Common:3; Rare:57 | ||||
| chr5:179820773-179820939 | Common:3; Rare:73; Clinvar:1; Clinvar (benign):2 | ||||
| chr5:179858798-179858969 | Rare:96 | ||||
| chr5:179907815-179908045 | Common:3; Rare:108 | ||||
| chr5:180802784-180802976 | Common:8; Rare:79 | ||||
| chr5:180810115-180810223 | Common:1; Rare:24 | ||||
| chr5:180861299-180861598 | Common:2; Rare:88 | ||||
| chr5:181223118-181223309 | Rare:64 | ||||
| chr5:181223559-181223749 | Common:3; Rare:44 | ||||
| chr5:181243690-181243730 | Rare:9 | ||||
| chr5:181261081-181261272 | Rare:65 |