| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:130181546-130181797 | Common:3; Rare:111 | ||||
| chr2:130182135-130182381 | Common:2; Rare:99 | ||||
| chr2:130342111-130342265 | Rare:68; Clinvar:1 | ||||
| chr2:130342645-130342935 | Common:5; Rare:91 | ||||
| chr2:131093382-131093559 | Common:1; Rare:83 | ||||
| chr2:131492754-131492972 | Common:5; Rare:72 | ||||
| chr2:131493033-131493097 | Common:1; Rare:16 | ||||
| chr2:134918585-134918863 | Common:1; Rare:110 | ||||
| chr2:135531178-135531543 | Common:1; Rare:76 | ||||
| chr2:135985404-135985670 | Common:4; Rare:119; Clinvar (benign):1 | ||||
| chr2:135985683-135985987 | Common:2; Rare:74 | ||||
| chr2:137964142-137964599 | Common:2; Rare:85 | ||||
| chr2:138501664-138502037 | Common:2; Rare:131 | ||||
| chr2:144517324-144517709 | Common:5; Rare:115; Clinvar:3; Clinvar (benign):4 | ||||
| chr2:144518134-144518334 | Common:2; Rare:53 |