| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:140175035-140175285 | Common:2; Rare:60 | ||||
| chr5:140303057-140303171 | Common:1; Rare:36 | ||||
| chr5:140346597-140346721 | Common:1; Rare:34 | ||||
| chr5:140401499-140401906 | Common:3; Rare:94 | ||||
| chr5:140547611-140547768 | Common:1; Rare:43 | ||||
| chr5:140557198-140557545 | Common:5; Rare:186 | ||||
| chr5:140562107-140562361 | Common:2; Rare:79 | ||||
| chr5:140564273-140564856 | Common:2; Rare:151 | ||||
| chr5:140592092-140592229 | Rare:28 | ||||
| chr5:140633036-140633444 | Common:1; Rare:73 | ||||
| chr5:140647551-140648084 | Common:19; Rare:209; Clinvar:4; Clinvar (benign):4 | ||||
| chr5:140664580-140664925 | Common:4; Rare:81 | ||||
| chr5:140691282-140691646 | Common:2; Rare:131; Clinvar:11; Clinvar (benign):2 | ||||
| chr5:141320732-141320921 | Common:2; Rare:65 | ||||
| chr5:141349993-141350160 | Rare:37 |