| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:124539026-124539245 | Common:2; Rare:112; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr8:124998182-124998617 | Common:4; Rare:169 | ||||
| chr8:125091710-125091910 | Common:2; Rare:70; Clinvar (benign):3 | ||||
| chr8:127735251-127735472 | Rare:35 | ||||
| chr8:127735922-127736458 | Common:3; Rare:128 | ||||
| chr8:129939622-129939990 | Common:1; Rare:128 | ||||
| chr8:133102857-133102942 | Rare:19 | ||||
| chr8:134713029-134713280 | Common:1; Rare:93 | ||||
| chr8:140511270-140511502 | Common:1; Rare:94 | ||||
| chr8:141001144-141001428 | Common:2; Rare:94 | ||||
| chr8:143334791-143334988 | Common:2; Rare:72 | ||||
| chr8:143541443-143541680 | Common:4; Rare:72 | ||||
| chr8:143635890-143636065 | Common:2; Rare:77 | ||||
| chr8:143684389-143684519 | Common:4; Rare:27 | ||||
| chr8:143791289-143791550 | Common:2; Rare:76 |