| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:87155240-87155606 | Rare:98 | ||||
| chr6:87472847-87473006 | Common:1; Rare:56; Clinvar (benign):4 | ||||
| chr6:87589920-87590169 | Common:3; Rare:127; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr6:87702214-87702528 | Common:1; Rare:97 | ||||
| chr6:88963540-88963830 | Common:2; Rare:96 | ||||
| chr6:89080586-89080880 | Common:2; Rare:125 | ||||
| chr6:89081049-89081416 | Common:2; Rare:138 | ||||
| chr6:89081491-89081841 | Common:4; Rare:117 | ||||
| chr6:89117943-89118115 | Common:2; Rare:76 | ||||
| chr6:89145919-89146132 | Rare:62 | ||||
| chr6:89352614-89353023 | Common:2; Rare:97 | ||||
| chr6:89412087-89412356 | Common:3; Rare:66 | ||||
| chr6:89638443-89638845 | Common:6; Rare:124 | ||||
| chr6:89819673-89819870 | Rare:65 | ||||
| chr6:89829594-89829981 | Common:1; Rare:99 |