Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:51120742-51120989 | Rare:102 | ||||
chr17:51153334-51153669 | Common:1; Rare:89 | ||||
chr17:51260409-51260587 | Common:3; Rare:91 | ||||
chr17:54968631-54968799 | Common:3; Rare:79 | ||||
chr17:55421782-55422174 | Common:3; Rare:127 | ||||
chr17:55751350-55751413 | Rare:25 | ||||
chr17:56914022-56914184 | Rare:41 | ||||
chr17:57084971-57085316 | Rare:117 | ||||
chr17:57850006-57850282 | Common:1; Rare:88 | ||||
chr17:57988180-57988512 | Common:5; Rare:99 | ||||
chr17:58219223-58219342 | Common:1; Rare:45; Clinvar:2; Clinvar (benign):3 | ||||
chr17:58352140-58352290 | Common:1; Rare:67 | ||||
chr17:58692530-58692663 | Common:1; Rare:72; Clinvar:9; Clinvar (benign):19 | ||||
chr17:59106707-59106970 | Common:2; Rare:86; Clinvar:4; Clinvar (benign):2 | ||||
chr17:59155122-59155545 | Common:2; Rare:103 |