| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:46394184-46394416 | Rare:66 | ||||
| chr1:46604143-46604502 | Common:3; Rare:165 | ||||
| chr1:46616749-46617081 | Common:5; Rare:120 | ||||
| chr1:46667710-46668210 | Common:2; Rare:235 | ||||
| chr1:46668280-46668684 | Common:7; Rare:293 | ||||
| chr1:46719016-46719439 | Common:4; Rare:390 | ||||
| chr1:46757130-46757590 | Common:1; Rare:183 | ||||
| chr1:46757610-46757990 | Common:4; Rare:188 | ||||
| chr1:46758061-46758371 | Common:2; Rare:81 | ||||
| chr1:46798760-46799080 | Common:3; Rare:94 | ||||
| chr1:46806530-46807805 | Common:13; Rare:357 | ||||
| chr1:47313998-47314576 | Common:12; Rare:356; Clinvar:9; Clinvar (benign):2 | ||||
| chr1:47333620-47334023 | Common:8; Rare:303 | ||||
| chr1:47334059-47334500 | Common:8; Rare:258 | ||||
| chr1:48472110-48472513 | Common:13; Rare:261 |