| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:98661495-98661863 | Common:3; Rare:129 | ||||
| chr1:99850006-99850128 | Common:1; Rare:46 | ||||
| chr1:99969922-99970074 | Rare:44 | ||||
| chr1:100037973-100038199 | Common:1; Rare:91 | ||||
| chr1:100132891-100133235 | Common:2; Rare:134 | ||||
| chr1:100249796-100250045 | Common:4; Rare:86; Clinvar:1; Clinvar (benign):1 | ||||
| chr1:100266114-100266419 | Common:3; Rare:107 | ||||
| chr1:100894658-100894914 | Common:1; Rare:62 | ||||
| chr1:100895938-100896155 | Rare:61 | ||||
| chr1:101025763-101025910 | Common:1; Rare:44 | ||||
| chr1:103108492-103108705 | Rare:53 | ||||
| chr1:107056468-107056791 | Common:2; Rare:130 | ||||
| chr1:108200098-108200414 | Common:7; Rare:104 | ||||
| chr1:108692197-108692344 | Common:1; Rare:52 | ||||
| chr1:108692549-108692598 | Common:3; Rare:35 |