| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:19311972-19312373 | Common:8; Rare:179 | ||||
| chr1:19596897-19597100 | Common:2; Rare:100 | ||||
| chr1:19799864-19800213 | Common:5; Rare:95 | ||||
| chr1:20185933-20186128 | Common:1; Rare:63 | ||||
| chr1:20588911-20589127 | Common:7; Rare:57 | ||||
| chr1:20661340-20661663 | Common:3; Rare:118; Clinvar:4; Clinvar (benign):6 | ||||
| chr1:20786602-20786859 | Rare:96 | ||||
| chr1:21176848-21177059 | Rare:59 | ||||
| chr1:21345463-21345670 | Common:2; Rare:79 | ||||
| chr1:21551063-21551398 | Common:1; Rare:60 | ||||
| chr1:21783086-21783272 | Common:2; Rare:66 | ||||
| chr1:22636528-22636735 | Common:1; Rare:44 | ||||
| chr1:23558954-23559138 | Common:4; Rare:88 | ||||
| chr1:23559407-23559648 | Common:1; Rare:103 | ||||
| chr1:23691590-23691829 | Common:3; Rare:76; Clinvar:2; Clinvar (benign):1 |