| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:130342100-130342281 | Rare:77; Clinvar:1 | ||||
| chr2:130342648-130342930 | Common:5; Rare:89 | ||||
| chr2:130355932-130356092 | Common:2; Rare:47 | ||||
| chr2:131093382-131093542 | Common:1; Rare:75 | ||||
| chr2:131105233-131105375 | Common:1; Rare:69 | ||||
| chr2:131492757-131493128 | Common:8; Rare:113 | ||||
| chr2:134918589-134918880 | Common:1; Rare:123 | ||||
| chr2:135531172-135531526 | Common:1; Rare:74 | ||||
| chr2:135985407-135985730 | Common:4; Rare:133; Clinvar (benign):1 | ||||
| chr2:138501661-138501971 | Common:2; Rare:115 | ||||
| chr2:144517317-144517684 | Common:5; Rare:110; Clinvar:3; Clinvar (benign):5 | ||||
| chr2:148020688-148021100 | Common:2; Rare:95; Clinvar (benign):2 | ||||
| chr2:148021571-148021671 | Rare:18 | ||||
| chr2:149587306-149587379 | Rare:14 | ||||
| chr2:149587662-149587822 | Common:1; Rare:50; Clinvar:2; Clinvar (benign):1 |