| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:144095433-144095456 | Rare:6 | ||||
| chr8:144096002-144096367 | Common:1; Rare:147; Clinvar (benign):4 | ||||
| chr8:144096419-144096741 | Common:1; Rare:117; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr8:144103647-144103875 | Common:1; Rare:77 | ||||
| chr8:144104159-144104526 | Common:3; Rare:125 | ||||
| chr8:144106201-144106394 | Rare:62 | ||||
| chr8:144148354-144148680 | Rare:62 | ||||
| chr8:144308803-144309007 | Rare:55 | ||||
| chr8:144309530-144309823 | Rare:87 | ||||
| chr8:144316857-144317145 | Rare:120; Clinvar (pathogenic):1 | ||||
| chr8:144317178-144317590 | Rare:156; Clinvar (pathogenic):1 | ||||
| chr8:144317657-144318024 | Common:2; Rare:131; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr8:144318285-144319072 | Common:5; Rare:301; Clinvar:1; Clinvar (benign):2 | ||||
| chr8:144395880-144395902 | Rare:8 | ||||
| chr8:144409295-144409435 | Rare:42 |