| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:139904453-139904720 | Common:1; Rare:70 | ||||
| chr5:140107998-140108172 | Rare:52 | ||||
| chr5:140174989-140175241 | Rare:73 | ||||
| chr5:140346601-140346715 | Common:1; Rare:32 | ||||
| chr5:140401433-140401869 | Common:3; Rare:86 | ||||
| chr5:140557405-140557493 | Rare:56 | ||||
| chr5:140564296-140564553 | Common:1; Rare:61 | ||||
| chr5:140564555-140564846 | Rare:76 | ||||
| chr5:140647579-140647924 | Common:5; Rare:141; Clinvar:4; Clinvar (benign):3 | ||||
| chr5:140691317-140691620 | Common:1; Rare:106; Clinvar:8; Clinvar (benign):1 | ||||
| chr5:141102193-141102323 | Common:2; Rare:56 | ||||
| chr5:141320742-141320898 | Common:1; Rare:49 | ||||
| chr5:141618917-141619246 | Common:1; Rare:105; Clinvar:5; Clinvar (benign):1 | ||||
| chr5:141636809-141637001 | Common:2; Rare:83 | ||||
| chr5:141682195-141682395 | Common:2; Rare:55 |