| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:131105208-131105361 | Common:1; Rare:66 | ||||
| chr2:131492754-131493089 | Common:8; Rare:100 | ||||
| chr2:134918588-134918857 | Common:1; Rare:106 | ||||
| chr2:135052218-135052325 | Common:1; Rare:46; Clinvar (benign):1 | ||||
| chr2:135531172-135531514 | Common:1; Rare:72 | ||||
| chr2:135876400-135876633 | Rare:63 | ||||
| chr2:135985429-135985690 | Common:4; Rare:117; Clinvar (benign):1 | ||||
| chr2:136118139-136118288 | Rare:40 | ||||
| chr2:136765450-136765579 | Common:4; Rare:38 | ||||
| chr2:138780350-138780517 | Rare:50 | ||||
| chr2:144332449-144332658 | Rare:84 | ||||
| chr2:144430770-144431088 | Rare:49 | ||||
| chr2:144517324-144517607 | Rare:80; Clinvar:3; Clinvar (benign):4 | ||||
| chr2:144517744-144517800 | Common:1; Rare:7 | ||||
| chr2:144518434-144518463 | Rare:5 |