| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:117367008-117367231 | Rare:52 | ||||
| chr1:117367276-117367483 | Common:4; Rare:75 | ||||
| chr1:117367898-117368093 | Common:1; Rare:40 | ||||
| chr1:117605723-117606105 | Common:2; Rare:118 | ||||
| chr1:117929543-117930007 | Common:5; Rare:130 | ||||
| chr1:119140168-119140491 | Common:2; Rare:84 | ||||
| chr1:119140509-119140939 | Common:1; Rare:133; Clinvar (pathogenic):1 | ||||
| chr1:119141109-119141157 | Rare:11 | ||||
| chr1:119647676-119647868 | Rare:29 | ||||
| chr1:119648093-119648453 | Common:4; Rare:109 | ||||
| chr1:119711786-119712146 | Common:2; Rare:108; Clinvar:6; Clinvar (benign):2 | ||||
| chr1:119712347-119712956 | Common:3; Rare:125 | ||||
| chr1:120069349-120069411 | Common:4; Rare:22; Clinvar:1; Clinvar (benign):2 | ||||
| chr1:120176149-120176286 | Common:1; Rare:22 | ||||
| chr1:120176313-120176688 | Common:1; Rare:67 |