Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:145719414-145719511 | Common:1; Rare:15 | ||||
chr1:145823927-145824259 | Rare:115 | ||||
chr1:145858992-145859175 | Rare:51 | ||||
chr1:145918680-145919023 | Common:2; Rare:79 | ||||
chr1:145927364-145927604 | Common:1; Rare:60; Clinvar (pathogenic):1 | ||||
chr1:145958007-145958223 | Rare:52 | ||||
chr1:145964571-145964748 | Rare:46 | ||||
chr1:145995528-145995851 | Common:1; Rare:109 | ||||
chr1:145995944-145996808 | Common:1; Rare:329 | ||||
chr1:147172119-147172336 | Rare:51 | ||||
chr1:147172421-147172823 | Common:1; Rare:103 | ||||
chr1:147225203-147225651 | Common:3; Rare:85 | ||||
chr1:147242541-147242746 | Common:4; Rare:89 | ||||
chr1:147541443-147541506 | Rare:3 | ||||
chr1:148458688-148459006 | Common:2; Rare:89 |