Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:11909587-11909797 | Common:3; Rare:105 | ||||
chr1:11909860-11910071 | Common:14; Rare:110 | ||||
chr1:12001640-12001823 | Common:1; Rare:48; Clinvar:1; Clinvar (benign):1 | ||||
chr1:12148331-12148580 | Common:1; Rare:37 | ||||
chr1:12381197-12381429 | Rare:23 | ||||
chr1:12381450-12381628 | Common:1; Rare:28 | ||||
chr1:12528401-12528546 | Rare:17 | ||||
chr1:12618553-12618720 | Common:1; Rare:35 | ||||
chr1:12619021-12619261 | Rare:51 | ||||
chr1:12619345-12619474 | Rare:23 | ||||
chr1:13708792-13708847 | Common:2; Rare:7 | ||||
chr1:14535726-14535827 | Rare:18 | ||||
chr1:14943378-14943433 | Common:1; Rare:12 | ||||
chr1:15090491-15090679 | Common:2; Rare:44 | ||||
chr1:15139798-15139866 | Common:2; Rare:13 |