Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:3636238-3636468 | Common:4; Rare:63; Clinvar (benign):1 | ||||
chr17:3668527-3668820 | Common:3; Rare:118 | ||||
chr17:3723781-3723853 | Common:1; Rare:42 | ||||
chr17:4142942-4143231 | Common:3; Rare:103 | ||||
chr17:4143640-4143777 | Common:4; Rare:80 | ||||
chr17:4263939-4264067 | Rare:53 | ||||
chr17:4555312-4555605 | Common:3; Rare:130 | ||||
chr17:4704104-4704211 | Rare:61 | ||||
chr17:4807006-4807183 | Common:3; Rare:59 | ||||
chr17:4939893-4940341 | Common:2; Rare:132 | ||||
chr17:4948939-4949194 | Common:2; Rare:85 | ||||
chr17:4987630-4987732 | Common:1; Rare:41 | ||||
chr17:5420054-5420217 | Rare:66 | ||||
chr17:5486164-5486403 | Common:4; Rare:102 | ||||
chr17:6640677-6641073 | Common:7; Rare:120 |