| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:78004552-78004873 | Common:3; Rare:80 | ||||
| chr1:84077893-84078133 | Common:1; Rare:91 | ||||
| chr1:84574453-84574553 | Common:1; Rare:25 | ||||
| chr1:84690418-84690688 | Rare:83 | ||||
| chr1:85276348-85276720 | Common:5; Rare:123 | ||||
| chr1:85708297-85708518 | Common:2; Rare:81 | ||||
| chr1:86396252-86396413 | Common:3; Rare:39 | ||||
| chr1:86704691-86704897 | Common:2; Rare:79 | ||||
| chr1:86914323-86914637 | Common:1; Rare:79 | ||||
| chr1:88684025-88684366 | Common:3; Rare:97 | ||||
| chr1:89994981-89995165 | Common:2; Rare:74 | ||||
| chr1:91500808-91500890 | Common:2; Rare:31 | ||||
| chr1:92029930-92030002 | Rare:23 | ||||
| chr1:92298927-92299076 | Common:1; Rare:73; Clinvar:2; Clinvar (benign):1 | ||||
| chr1:93079097-93079308 | Common:2; Rare:88 |