| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:134371027-134371190 | Common:1; Rare:42 | ||||
| chr5:134525544-134525676 | Rare:31 | ||||
| chr5:134648726-134648949 | Common:1; Rare:51 | ||||
| chr5:138033025-138033331 | Common:1; Rare:87 | ||||
| chr5:138178598-138178739 | Rare:35 | ||||
| chr5:138178935-138179187 | Common:3; Rare:51 | ||||
| chr5:138213313-138213551 | Rare:52 | ||||
| chr5:138331792-138332122 | Common:1; Rare:80 | ||||
| chr5:138543104-138543490 | Common:2; Rare:115 | ||||
| chr5:138930650-138930837 | Rare:44 | ||||
| chr5:140564335-140564847 | Common:1; Rare:130 | ||||
| chr5:140647567-140647871 | Common:5; Rare:125; Clinvar:4; Clinvar (benign):3 | ||||
| chr5:140691263-140691481 | Common:2; Rare:79; Clinvar:7; Clinvar (benign):1 | ||||
| chr5:141320722-141320886 | Common:2; Rare:51 | ||||
| chr5:141636815-141637025 | Common:1; Rare:85 |