| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:156126704-156127104 | Common:2; Rare:139 | ||||
| chr1:156193711-156194153 | Common:3; Rare:99 | ||||
| chr1:156212835-156213068 | Common:1; Rare:68 | ||||
| chr1:156213176-156213379 | Common:2; Rare:58 | ||||
| chr1:156282206-156282611 | Common:2; Rare:88 | ||||
| chr1:156282777-156283076 | Common:2; Rare:68 | ||||
| chr1:156338178-156338643 | Common:4; Rare:158 | ||||
| chr1:156338684-156338904 | Rare:60 | ||||
| chr1:156369115-156369245 | Common:2; Rare:40 | ||||
| chr1:156419886-156420286 | Common:1; Rare:111 | ||||
| chr1:156421738-156421945 | Common:1; Rare:60 | ||||
| chr1:156500768-156501067 | Common:1; Rare:107 | ||||
| chr1:156572518-156572640 | Rare:46 | ||||
| chr1:156591647-156591816 | Common:4; Rare:87 | ||||
| chr1:156591948-156592081 | Rare:44; Clinvar (pathogenic):1 |