| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:244051167-244051317 | Rare:12 | ||||
| chr1:244451815-244451931 | Rare:39 | ||||
| chr1:244451968-244452360 | Common:2; Rare:114 | ||||
| chr1:244461205-244461279 | Rare:25 | ||||
| chr1:244461304-244461586 | Common:2; Rare:94 | ||||
| chr1:244652489-244653193 | Common:7; Rare:221 | ||||
| chr1:244653307-244653358 | Rare:18 | ||||
| chr1:244653763-244653821 | Rare:15 | ||||
| chr1:244835788-244835882 | Common:2; Rare:35 | ||||
| chr1:244862960-244863202 | Common:3; Rare:96 | ||||
| chr1:244863212-244863474 | Common:6; Rare:104 | ||||
| chr1:244863576-244863802 | Rare:84; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr1:244864340-244864824 | Common:1; Rare:194 | ||||
| chr1:244864902-244865172 | Common:1; Rare:62 | ||||
| chr1:244969664-244970269 | Common:2; Rare:201 |