| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:177133503-177133872 | Rare:134 | ||||
| chr5:177303706-177304008 | Common:3; Rare:119 | ||||
| chr5:177600021-177600159 | Common:3; Rare:43 | ||||
| chr5:179559534-179559771 | Common:1; Rare:65 | ||||
| chr5:179698709-179699009 | Common:2; Rare:98 | ||||
| chr5:179820668-179820918 | Common:6; Rare:78; Clinvar (benign):2 | ||||
| chr5:179858797-179858928 | Rare:73 | ||||
| chr5:180861249-180861574 | Common:2; Rare:103 | ||||
| chr6:2245438-2245820 | Common:1; Rare:130 | ||||
| chr6:2962098-2962263 | Common:1; Rare:35 | ||||
| chr6:5260900-5260998 | Common:1; Rare:33 | ||||
| chr6:5261224-5261553 | Common:11; Rare:81 | ||||
| chr6:7389740-7389849 | Common:1; Rare:34 | ||||
| chr6:10694607-10694988 | Common:4; Rare:101 | ||||
| chr6:10722796-10723204 | Common:5; Rare:135 |