| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:24952372-24952772 | Common:5; Rare:124 | ||||
| chr10:24952790-24953520 | Common:2; Rare:265 | ||||
| chr10:25016321-25016781 | Common:20; Rare:295 | ||||
| chr10:25016927-25017190 | Common:14; Rare:278 | ||||
| chr10:25174510-25174870 | Rare:79 | ||||
| chr10:25465940-25466245 | Common:4; Rare:160 | ||||
| chr10:26696920-26697264 | Common:1; Rare:95 | ||||
| chr10:26697200-26697525 | Common:9; Rare:146 | ||||
| chr10:26697479-26697789 | Common:3; Rare:173; Clinvar (benign):4 | ||||
| chr10:26697770-26698140 | Common:10; Rare:178; Clinvar:4; Clinvar (benign):3 | ||||
| chr10:26860764-26861320 | Common:13; Rare:357 | ||||
| chr10:27100376-27100678 | Common:13; Rare:211; Clinvar:12; Clinvar (benign):8 | ||||
| chr10:27154127-27154526 | Common:2; Rare:250 | ||||
| chr10:27155087-27155446 | Common:20; Rare:347; Clinvar:15; Clinvar (benign):20 | ||||
| chr10:27155844-27156245 | Common:8; Rare:86 |