| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:140971009-140971311 | Common:3; Rare:61 | ||||
| chr8:140975435-140975506 | Common:1; Rare:12 | ||||
| chr8:141129684-141129733 | Rare:7 | ||||
| chr8:143280843-143281120 | Common:3; Rare:48 | ||||
| chr8:143718829-143719017 | Common:2; Rare:87 | ||||
| chr8:143782527-143782766 | Rare:65 | ||||
| chr8:143817685-143817896 | Rare:48 | ||||
| chr8:143895877-143896122 | Common:2; Rare:39 | ||||
| chr8:143929240-143929568 | Common:1; Rare:153; Clinvar:14; Clinvar (benign):6 | ||||
| chr8:143929646-143930062 | Common:3; Rare:191; Clinvar:17; Clinvar (benign):11 | ||||
| chr8:143931937-143932237 | Common:2; Rare:153; Clinvar:13; Clinvar (benign):7 | ||||
| chr8:143933759-143934094 | Common:12; Rare:110; Clinvar:8; Clinvar (benign):5 | ||||
| chr8:143934160-143934460 | Common:3; Rare:112; Clinvar:6; Clinvar (benign):6 | ||||
| chr8:143934635-143935320 | Common:3; Rare:273; Clinvar:19; Clinvar (benign):20 | ||||
| chr8:143935481-143936054 | Common:1; Rare:158; Clinvar:3; Clinvar (benign):6 |