| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:31101242-31101602 | Common:11; Rare:97 | ||||
| chr18:31101919-31102016 | Common:1; Rare:27; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr18:31498082-31498259 | Common:1; Rare:57; Clinvar:4; Clinvar (benign):5 | ||||
| chr18:31943087-31943372 | Common:7; Rare:92 | ||||
| chr18:32092627-32092754 | Common:2; Rare:74 | ||||
| chr18:34976965-34977067 | Common:1; Rare:14 | ||||
| chr18:35240909-35241094 | Common:2; Rare:69 | ||||
| chr18:35290193-35290423 | Common:3; Rare:79 | ||||
| chr18:35344388-35344507 | Common:2; Rare:39 | ||||
| chr18:35972462-35972736 | Common:3; Rare:93 | ||||
| chr18:36129203-36129551 | Common:4; Rare:110 | ||||
| chr18:36129788-36130029 | Common:3; Rare:93 | ||||
| chr18:36187362-36187577 | Common:4; Rare:74 | ||||
| chr18:36828731-36829280 | Common:3; Rare:214 | ||||
| chr18:44680735-44680957 | Common:1; Rare:68; Clinvar:2; Clinvar (benign):1 |