| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:130182078-130182279 | Common:1; Rare:71 | ||||
| chr2:130342123-130342232 | Rare:45; Clinvar:1 | ||||
| chr2:130342679-130342939 | Common:3; Rare:87 | ||||
| chr2:130346232-130346515 | Common:2; Rare:103 | ||||
| chr2:130355929-130356117 | Common:2; Rare:55 | ||||
| chr2:130372556-130372760 | Common:1; Rare:57 | ||||
| chr2:131093293-131093549 | Common:1; Rare:107 | ||||
| chr2:131492719-131493105 | Common:8; Rare:116 | ||||
| chr2:134918656-134919001 | Common:1; Rare:137 | ||||
| chr2:135531184-135531627 | Common:1; Rare:96 | ||||
| chr2:135985404-135985708 | Common:4; Rare:131; Clinvar (benign):1 | ||||
| chr2:137964095-137964520 | Common:2; Rare:71 | ||||
| chr2:138501628-138501812 | Common:3; Rare:81 | ||||
| chr2:144517505-144517788 | Common:5; Rare:70 | ||||
| chr2:147844465-147844517 | Rare:19 |