| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:116910355-116910739 | Common:2; Rare:104 | ||||
| chr1:117059689-117060424 | Common:26; Rare:454 | ||||
| chr1:117121060-117121620 | Common:12; Rare:287 | ||||
| chr1:117121601-117122334 | Common:9; Rare:481 | ||||
| chr1:117122412-117123063 | Common:10; Rare:222 | ||||
| chr1:117210824-117211096 | Common:7; Rare:130 | ||||
| chr1:117211150-117211400 | Common:1; Rare:45 | ||||
| chr1:117366565-117366971 | Common:2; Rare:220 | ||||
| chr1:117367223-117367603 | Common:18; Rare:311 | ||||
| chr1:117367891-117368648 | Common:2; Rare:216 | ||||
| chr1:117605694-117606132 | Common:3; Rare:330 | ||||
| chr1:117929522-117929902 | Common:12; Rare:296 | ||||
| chr1:118081270-118081884 | Common:5; Rare:342 | ||||
| chr1:118185154-118185460 | Common:1; Rare:115 | ||||
| chr1:119140517-119140887 | Common:3; Rare:263; Clinvar (pathogenic):2 |