| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:109483623-109484046 | Common:19; Rare:357 | ||||
| chr1:109484046-109484446 | Common:3; Rare:164 | ||||
| chr1:109493801-109494498 | Common:11; Rare:392 | ||||
| chr1:109509587-109509987 | Common:4; Rare:376 | ||||
| chr1:109548040-109548154 | Rare:20 | ||||
| chr1:109548094-109548703 | Common:24; Rare:574 | ||||
| chr1:109548795-109549221 | Common:4; Rare:169; Clinvar (pathogenic):2 | ||||
| chr1:109615861-109616261 | Common:2; Rare:69 | ||||
| chr1:109618539-109619204 | Common:2; Rare:122 | ||||
| chr1:109619478-109619998 | Common:4; Rare:400 | ||||
| chr1:109620128-109620818 | Common:6; Rare:272 | ||||
| chr1:109620900-109621260 | Common:1; Rare:171; Clinvar:2; Clinvar (benign):1 | ||||
| chr1:109655937-109656498 | Common:13; Rare:528 | ||||
| chr1:109667784-109668184 | Common:9; Rare:290 | ||||
| chr1:109740169-109740569 | Common:5; Rare:313 |