| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:134004647-134004890 | Common:1; Rare:91 | ||||
| chr5:134226043-134226406 | Common:1; Rare:115 | ||||
| chr5:134371026-134371184 | Common:1; Rare:41 | ||||
| chr5:134648726-134648859 | Rare:38 | ||||
| chr5:134738193-134738567 | Common:1; Rare:114 | ||||
| chr5:136046976-136047349 | Common:2; Rare:89; Clinvar:2; Clinvar (benign):1 | ||||
| chr5:138178946-138179190 | Common:3; Rare:49 | ||||
| chr5:138543110-138543312 | Common:1; Rare:64 | ||||
| chr5:140564302-140564466 | Common:1; Rare:47 | ||||
| chr5:140564558-140564845 | Rare:76 | ||||
| chr5:140647591-140647880 | Common:5; Rare:119; Clinvar:4; Clinvar (benign):3 | ||||
| chr5:140691273-140691461 | Common:2; Rare:70; Clinvar:6; Clinvar (benign):1 | ||||
| chr5:141320723-141320902 | Common:2; Rare:59 | ||||
| chr5:141636815-141636985 | Common:1; Rare:74 | ||||
| chr5:141682184-141682408 | Common:2; Rare:63 |