| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:92831861-92832194 | Common:1; Rare:145; Clinvar:7; Clinvar (benign):7 | ||||
| chr1:92961343-92961909 | Common:4; Rare:167 | ||||
| chr1:93079017-93079379 | Common:4; Rare:146 | ||||
| chr1:93079771-93079940 | Rare:24 | ||||
| chr1:93179744-93179812 | Rare:12 | ||||
| chr1:93179859-93180014 | Common:1; Rare:42 | ||||
| chr1:93180295-93180848 | Common:2; Rare:223 | ||||
| chr1:93181069-93181223 | Common:1; Rare:22 | ||||
| chr1:93345701-93345993 | Common:4; Rare:109 | ||||
| chr1:93346249-93346644 | Common:2; Rare:96 | ||||
| chr1:93681776-93682053 | Common:4; Rare:76 | ||||
| chr1:93846542-93846828 | Common:1; Rare:100 | ||||
| chr1:93847148-93847294 | Common:1; Rare:35 | ||||
| chr1:93847485-93847634 | Common:1; Rare:66 | ||||
| chr1:93879092-93879371 | Common:3; Rare:104 |