Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:34424754-34425195 | Common:3; Rare:115; Clinvar (benign):6 | ||||
chr6:34696385-34696474 | Common:1; Rare:24 | ||||
chr6:34696488-34696574 | Rare:23 | ||||
chr6:34696709-34696980 | Common:1; Rare:61 | ||||
chr6:34757315-34757550 | Common:1; Rare:68 | ||||
chr6:35259405-35259778 | Common:3; Rare:117 | ||||
chr6:35688802-35689146 | Common:1; Rare:118 | ||||
chr6:35689230-35689317 | Rare:13 | ||||
chr6:35728006-35728245 | Rare:46 | ||||
chr6:35728327-35728416 | Rare:16 | ||||
chr6:35921042-35921261 | Common:1; Rare:92 | ||||
chr6:36679229-36679451 | Rare:30 | ||||
chr6:36874768-36874902 | Rare:48 | ||||
chr6:37257615-37257820 | Rare:55 | ||||
chr6:38639905-38639976 | Rare:19 |