| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:85708283-85708498 | Common:2; Rare:75 | ||||
| chr1:86704470-86704968 | Common:3; Rare:179 | ||||
| chr1:86914326-86914755 | Common:1; Rare:129 | ||||
| chr1:88684109-88684314 | Common:2; Rare:53 | ||||
| chr1:88992588-88992976 | Common:3; Rare:100 | ||||
| chr1:89198851-89198987 | Rare:21 | ||||
| chr1:89632894-89633196 | Common:1; Rare:85 | ||||
| chr1:89994981-89995193 | Common:2; Rare:80 | ||||
| chr1:91886019-91886340 | Rare:130 | ||||
| chr1:92298945-92299076 | Common:1; Rare:66; Clinvar:1; Clinvar (benign):1 | ||||
| chr1:92784967-92785265 | Common:4; Rare:110 | ||||
| chr1:92792395-92792543 | Common:1; Rare:29 | ||||
| chr1:93079125-93079298 | Common:2; Rare:70 | ||||
| chr1:93179622-93179922 | Common:2; Rare:49 | ||||
| chr1:93180051-93180103 | Rare:19 |