Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:138557410-138557606 | Rare:50 | ||||
chr5:138575654-138575832 | Rare:48 | ||||
chr5:138753280-138753504 | Common:2; Rare:75 | ||||
chr5:139198289-139198525 | Rare:79; Clinvar (benign):1 | ||||
chr5:139273975-139274150 | Rare:83 | ||||
chr5:139561112-139561397 | Common:1; Rare:113 | ||||
chr5:139561723-139561802 | Rare:35 | ||||
chr5:139648190-139648359 | Rare:49 | ||||
chr5:140107611-140107856 | Rare:87 | ||||
chr5:140174893-140175241 | Rare:103 | ||||
chr5:140346590-140346721 | Common:1; Rare:36 | ||||
chr5:140547467-140547719 | Common:2; Rare:55 | ||||
chr5:140564309-140564511 | Common:1; Rare:53 | ||||
chr5:140564550-140564837 | Rare:75 | ||||
chr5:140633064-140633505 | Common:1; Rare:74 |