| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:140647579-140647892 | Common:5; Rare:129; Clinvar:4; Clinvar (benign):3 | ||||
| chr5:140664560-140664910 | Common:4; Rare:79 | ||||
| chr5:140691273-140691481 | Common:2; Rare:77; Clinvar:7; Clinvar (benign):1 | ||||
| chr5:141320739-141320912 | Common:2; Rare:58 | ||||
| chr5:141636808-141637011 | Common:2; Rare:87 | ||||
| chr5:141682180-141682381 | Common:2; Rare:58 | ||||
| chr5:141923736-141923910 | Common:1; Rare:50 | ||||
| chr5:142109002-142109004 | |||||
| chr5:142770373-142770532 | Common:2; Rare:47 | ||||
| chr5:142770897-142771131 | Common:1; Rare:67 | ||||
| chr5:143404380-143404604 | Common:3; Rare:64 | ||||
| chr5:148383771-148384029 | Rare:76 | ||||
| chr5:149550296-149550453 | Rare:24 | ||||
| chr5:149551353-149551608 | Rare:59 | ||||
| chr5:150412595-150412947 | Common:1; Rare:95 |