| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:110407616-110407845 | Common:4; Rare:101 | ||||
| chr1:111140069-111140259 | Common:1; Rare:66 | ||||
| chr1:112395966-112396262 | Common:2; Rare:93 | ||||
| chr1:112619101-112619205 | Rare:37 | ||||
| chr1:112619634-112619877 | Common:2; Rare:86 | ||||
| chr1:112674567-112674758 | Common:1; Rare:35 | ||||
| chr1:112956190-112956437 | Common:4; Rare:112; Clinvar:8; Clinvar (benign):3 | ||||
| chr1:113905025-113905381 | Common:4; Rare:99 | ||||
| chr1:117060050-117060360 | Common:6; Rare:82 | ||||
| chr1:117929555-117929800 | Common:2; Rare:73 | ||||
| chr1:119140640-119140767 | Rare:38 | ||||
| chr1:120176380-120176620 | Common:1; Rare:53 | ||||
| chr1:145823895-145824251 | Rare:126 | ||||
| chr1:145918700-145919005 | Common:2; Rare:61 | ||||
| chr1:145927431-145927644 | Common:1; Rare:61; Clinvar (pathogenic):1 |