| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:134648720-134648850 | Rare:35 | ||||
| chr5:134738335-134738615 | Rare:104 | ||||
| chr5:134758646-134758820 | Common:1; Rare:52 | ||||
| chr5:134845915-134846089 | Rare:86 | ||||
| chr5:134905070-134905174 | Common:1; Rare:26 | ||||
| chr5:136053676-136054011 | Common:2; Rare:73 | ||||
| chr5:138033065-138033175 | Common:1; Rare:38 | ||||
| chr5:138178953-138179178 | Common:2; Rare:47 | ||||
| chr5:138331759-138332110 | Common:2; Rare:88 | ||||
| chr5:138337761-138338104 | Common:3; Rare:107 | ||||
| chr5:138543110-138543513 | Common:2; Rare:125 | ||||
| chr5:138753273-138753503 | Common:2; Rare:79 | ||||
| chr5:139273873-139274135 | Common:1; Rare:112; Clinvar:1; Clinvar (benign):2 | ||||
| chr5:139404029-139404283 | Rare:76 | ||||
| chr5:139462627-139462838 | Rare:48 |