| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:55227010-55227880 | Common:10; Rare:543; Clinvar (benign):2 | ||||
| chr5:55232485-55233222 | Common:4; Rare:216; Clinvar (benign):3 | ||||
| chr5:55233420-55233990 | Common:21; Rare:500; Clinvar:1 | ||||
| chr5:55306803-55307064 | Common:1; Rare:46 | ||||
| chr5:55307536-55308068 | Common:32; Rare:1004 | ||||
| chr5:55308024-55308603 | Common:3; Rare:231 | ||||
| chr5:55712170-55712720 | Common:9; Rare:356 | ||||
| chr5:55994840-55995319 | Rare:940 | ||||
| chr5:55995401-55995801 | Rare:112 | ||||
| chr5:56116686-56116810 | Common:1; Rare:35 | ||||
| chr5:56116827-56117227 | Common:8; Rare:120 | ||||
| chr5:56814645-56815190 | Common:11; Rare:309 | ||||
| chr5:56815120-56815805 | Common:25; Rare:868; Clinvar (benign):3 | ||||
| chr5:56908583-56908983 | Common:1; Rare:92 | ||||
| chr5:56909199-56909750 | Common:25; Rare:603 |