| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:134758630-134758829 | Common:2; Rare:64 | ||||
| chr5:134905045-134905208 | Common:1; Rare:45 | ||||
| chr5:135399061-135399316 | Rare:65 | ||||
| chr5:138032991-138033170 | Common:1; Rare:61 | ||||
| chr5:138178920-138179112 | Common:1; Rare:43 | ||||
| chr5:138352476-138352720 | Common:2; Rare:68 | ||||
| chr5:138465792-138466049 | Rare:116 | ||||
| chr5:138543110-138543501 | Common:2; Rare:117 | ||||
| chr5:138543740-138543793 | Rare:14 | ||||
| chr5:138575232-138575742 | Common:2; Rare:196 | ||||
| chr5:138753290-138753457 | Common:2; Rare:48 | ||||
| chr5:139198255-139198550 | Rare:93; Clinvar (benign):1 | ||||
| chr5:139293579-139293803 | Rare:74 | ||||
| chr5:139389678-139389720 | Rare:10 | ||||
| chr5:139561124-139561387 | Common:1; Rare:107 |