Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:181243685-181243960 | Common:4; Rare:98 | ||||
chr5:181244174-181244482 | Common:3; Rare:59 | ||||
chr5:181261087-181261207 | Rare:37 | ||||
chr6:1311797-1312138 | Common:3; Rare:105 | ||||
chr6:2245588-2245833 | Rare:78 | ||||
chr6:2902811-2902947 | Rare:25 | ||||
chr6:2971251-2971552 | Common:5; Rare:70 | ||||
chr6:2971561-2971716 | Common:1; Rare:44 | ||||
chr6:3118366-3118737 | Common:5; Rare:120 | ||||
chr6:3227636-3227943 | Rare:75 | ||||
chr6:3849145-3849444 | Common:3; Rare:84 | ||||
chr6:4021200-4021455 | Rare:112 | ||||
chr6:5003610-5003843 | Common:6; Rare:72 | ||||
chr6:5003994-5004126 | Common:2; Rare:59 | ||||
chr6:5260650-5261059 | Common:5; Rare:149; Clinvar (benign):4 |