| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:114281760-114282200 | Common:8; Rare:219 | ||||
| chr13:114282311-114282711 | Common:4; Rare:122 | ||||
| chr13:114314226-114314542 | Rare:95 | ||||
| chr14:20333260-20333435 | Common:1; Rare:34 | ||||
| chr14:20343055-20343650 | Common:13; Rare:320 | ||||
| chr14:20413085-20413210 | Common:1; Rare:17 | ||||
| chr14:20413417-20413581 | Common:3; Rare:50 | ||||
| chr14:20454744-20455307 | Common:7; Rare:148 | ||||
| chr14:20461380-20461750 | Common:3; Rare:110 | ||||
| chr14:20469291-20469462 | Common:1; Rare:33; Clinvar:2; Clinvar (benign):1 | ||||
| chr14:20469564-20470270 | Common:3; Rare:182 | ||||
| chr14:20683707-20684011 | Common:8; Rare:73 | ||||
| chr14:20684303-20685001 | Common:11; Rare:226; Clinvar:5; Clinvar (benign):10 | ||||
| chr14:20989622-20990039 | Common:8; Rare:106 | ||||
| chr14:20990417-20990528 | Common:2; Rare:37 |