| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:37748002-37748068 | Rare:28 | ||||
| chr8:49168407-49168523 | Rare:25 | ||||
| chr8:74199259-74199423 | Rare:28 | ||||
| chr8:123653770-123653953 | Rare:40 | ||||
| chr8:129148523-129148714 | Common:3; Rare:44 | ||||
| chr8:133256793-133257063 | Common:1; Rare:62; Clinvar:1; Clinvar (benign):1 | ||||
| chr8:143281635-143281809 | Common:3; Rare:41 | ||||
| chr8:144700524-144700656 | Common:2; Rare:26 | ||||
| chr8:145002827-145002948 | Common:1; Rare:37 | ||||
| chr9:35341744-35341879 | Common:1; Rare:23 | ||||
| chr9:35684247-35684809 | Rare:138; Clinvar:4; Clinvar (benign):5 | ||||
| chr9:40106592-40106734 | Common:2; Rare:17 | ||||
| chr9:40991967-40992351 | Common:7; Rare:30 | ||||
| chr9:62897703-62897718 | Rare:5 | ||||
| chr9:66269890-66270062 | Common:1; Rare:31 |