| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:1019743-1020379 | Common:6; Rare:275; Clinvar:7; Clinvar (benign):2 | ||||
| chr1:1020585-1020988 | Common:8; Rare:122 | ||||
| chr1:1073560-1074545 | Common:21; Rare:494 | ||||
| chr1:1115964-1116539 | Common:4; Rare:365 | ||||
| chr1:1231170-1231821 | Common:3; Rare:211 | ||||
| chr1:1231883-1232409 | Rare:517; Clinvar:12; Clinvar (benign):12; Clinvar (pathogenic):5 | ||||
| chr1:1232430-1232894 | Common:1; Rare:208; Clinvar:14; Clinvar (benign):5; Clinvar (pathogenic):4 | ||||
| chr1:1273414-1273667 | Common:1; Rare:82 | ||||
| chr1:1273748-1274090 | Common:5; Rare:317 | ||||
| chr1:1304543-1305336 | Common:8; Rare:388 | ||||
| chr1:1307377-1307777 | Common:5; Rare:185 | ||||
| chr1:1307831-1308195 | Rare:197 | ||||
| chr1:1308284-1308828 | Common:22; Rare:483 | ||||
| chr1:1309630-1310080 | Common:6; Rare:340 | ||||
| chr1:1324576-1324986 | Common:9; Rare:525 |