| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:155127661-155128312 | Common:3; Rare:292 | ||||
| chr1:155129130-155129520 | Rare:84 | ||||
| chr1:155129850-155130229 | Common:4; Rare:245 | ||||
| chr1:155135054-155135522 | Common:2; Rare:298 | ||||
| chr1:155135565-155136079 | Common:11; Rare:414 | ||||
| chr1:155140041-155140248 | Rare:55; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr1:155140430-155140563 | Common:2; Rare:84; Clinvar (benign):8 | ||||
| chr1:155172886-155173066 | Common:1; Rare:44 | ||||
| chr1:155173142-155173453 | Common:9; Rare:356 | ||||
| chr1:155192750-155193171 | Common:1; Rare:247 | ||||
| chr1:155193309-155193856 | Rare:260 | ||||
| chr1:155199464-155200363 | Common:1; Rare:283 | ||||
| chr1:155207794-155208194 | Common:1; Rare:150 | ||||
| chr1:155208260-155208940 | Rare:257 | ||||
| chr1:155209080-155209305 | Rare:271 |