Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:149636386-149636599 | Common:7; Rare:68 | ||||
chr1:150515583-150515785 | Rare:62 | ||||
chr1:150561323-150561486 | Common:1; Rare:46 | ||||
chr1:151364914-151365285 | Common:1; Rare:101 | ||||
chr1:151366418-151366739 | Rare:78; Clinvar (pathogenic):1 | ||||
chr1:151830755-151830979 | Common:3; Rare:45 | ||||
chr1:153783715-153783855 | Common:4; Rare:51 | ||||
chr1:154182147-154182467 | Common:1; Rare:58 | ||||
chr1:154387181-154387352 | Rare:23 | ||||
chr1:154967742-154967994 | Rare:59 | ||||
chr1:155091338-155091669 | Common:2; Rare:59 | ||||
chr1:155126012-155126367 | Common:1; Rare:70 | ||||
chr1:155227531-155227712 | Common:1; Rare:49 | ||||
chr1:155980141-155980257 | Rare:16 | ||||
chr1:156749761-156749979 | Common:2; Rare:43 |