Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:149887007-149887166 | Common:1; Rare:67 | ||||
chr1:149887921-149888215 | Rare:82 | ||||
chr1:149927756-149927910 | Common:1; Rare:62; Clinvar (benign):5 | ||||
chr1:150067589-150067918 | Common:1; Rare:94 | ||||
chr1:150150169-150150219 | Common:1; Rare:14 | ||||
chr1:150234642-150234750 | Rare:22 | ||||
chr1:150364572-150364717 | Common:1; Rare:51 | ||||
chr1:150579157-150579271 | Rare:49 | ||||
chr1:150579582-150579830 | Common:9; Rare:82 | ||||
chr1:150629426-150629825 | Rare:91 | ||||
chr1:150876551-150876981 | Common:5; Rare:152 | ||||
chr1:151048017-151048237 | Rare:77 | ||||
chr1:151165829-151166171 | Common:3; Rare:95 | ||||
chr1:151281966-151282330 | Rare:100 | ||||
chr1:151763448-151763525 | Common:1; Rare:28 |