| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:144286100-144286500 | Common:10; Rare:148 | ||||
| chr6:145734450-145735040 | Common:7; Rare:212 | ||||
| chr6:145735193-145735329 | Common:2; Rare:90; Clinvar:12; Clinvar (benign):3 | ||||
| chr6:145735410-145735750 | Common:7; Rare:127; Clinvar:3; Clinvar (benign):9 | ||||
| chr6:145814630-145815100 | Common:3; Rare:315 | ||||
| chr6:145964293-145964479 | Common:1; Rare:106 | ||||
| chr6:146543471-146543850 | Common:13; Rare:201 | ||||
| chr6:147203434-147204321 | Common:5; Rare:245 | ||||
| chr6:147204530-147204900 | Common:1; Rare:127 | ||||
| chr6:148342525-148342888 | Rare:177 | ||||
| chr6:148342935-148343068 | Rare:27 | ||||
| chr6:148746757-148747092 | Common:2; Rare:174 | ||||
| chr6:148747690-148748310 | Common:5; Rare:301 | ||||
| chr6:149545998-149546159 | Rare:129 | ||||
| chr6:149566037-149566408 | Common:1; Rare:99 |