| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:18902710-18903030 | Common:11; Rare:140 | ||||
| chr1:18956657-18956945 | Common:2; Rare:77 | ||||
| chr1:19210104-19210560 | Common:1; Rare:202 | ||||
| chr1:19251471-19252039 | Common:15; Rare:297 | ||||
| chr1:19312034-19312369 | Common:16; Rare:315 | ||||
| chr1:19485440-19485799 | Common:1; Rare:241 | ||||
| chr1:19485800-19486090 | Common:2; Rare:120 | ||||
| chr1:19596730-19597102 | Common:6; Rare:262 | ||||
| chr1:19644171-19644392 | Common:6; Rare:117 | ||||
| chr1:19799550-19800250 | Common:13; Rare:285 | ||||
| chr1:19882215-19882501 | Common:4; Rare:156 | ||||
| chr1:20507580-20507980 | Common:2; Rare:153 | ||||
| chr1:20508028-20508240 | Common:4; Rare:144 | ||||
| chr1:20588762-20589142 | Common:11; Rare:125 | ||||
| chr1:20661348-20661727 | Common:6; Rare:265; Clinvar:8; Clinvar (benign):12 |