| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:122980407-122980950 | Common:2; Rare:165 | ||||
| chr12:123233096-123233486 | Common:2; Rare:126; Clinvar:1 | ||||
| chr12:123584314-123584595 | Common:6; Rare:87 | ||||
| chr12:123633624-123633851 | Common:1; Rare:104; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:124388807-124389018 | Common:3; Rare:60 | ||||
| chr12:130871735-130872122 | Common:4; Rare:161 | ||||
| chr12:131710795-131711105 | Rare:81 | ||||
| chr12:132887564-132887779 | Rare:65 | ||||
| chr13:21140401-21140614 | Rare:102 | ||||
| chr13:21176396-21176708 | Common:3; Rare:135 | ||||
| chr13:23889348-23889477 | Rare:48 | ||||
| chr13:24512732-24512870 | Common:3; Rare:41 | ||||
| chr13:24922795-24923039 | Common:1; Rare:77; Clinvar:1 | ||||
| chr13:26221814-26221918 | Rare:28 | ||||
| chr13:27251258-27251617 | Common:4; Rare:105 |