| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:156290740-156291581 | Common:2; Rare:254 | ||||
| chr1:156295168-156295280 | Rare:16 | ||||
| chr1:156295620-156295749 | Common:1; Rare:47 | ||||
| chr1:156337424-156338095 | Common:4; Rare:201 | ||||
| chr1:156338127-156338649 | Common:9; Rare:490 | ||||
| chr1:156338697-156338918 | Rare:61 | ||||
| chr1:156368870-156369292 | Common:7; Rare:209 | ||||
| chr1:156421677-156421918 | Common:1; Rare:65 | ||||
| chr1:156421826-156422786 | Common:5; Rare:212 | ||||
| chr1:156500668-156501169 | Common:7; Rare:446 | ||||
| chr1:156572467-156572603 | Common:1; Rare:55 | ||||
| chr1:156591603-156591878 | Common:16; Rare:328 | ||||
| chr1:156591890-156592183 | Rare:190; Clinvar (pathogenic):4 | ||||
| chr1:156592219-156593020 | Common:4; Rare:334; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr1:156601357-156601638 | Common:4; Rare:182 |