Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:53327149-53327565 | Common:8; Rare:142 | ||||
chr1:53327929-53328279 | Common:5; Rare:231 | ||||
chr1:53328320-53329060 | Common:10; Rare:185 | ||||
chr1:53837990-53838900 | Common:8; Rare:417 | ||||
chr1:53889691-53890025 | Common:4; Rare:184 | ||||
chr1:53893851-53894314 | Common:1; Rare:125 | ||||
chr1:53945502-53946153 | Common:21; Rare:445 | ||||
chr1:53946216-53946564 | Common:5; Rare:289 | ||||
chr1:54053149-54053746 | Common:18; Rare:521 | ||||
chr1:54199877-54200308 | Rare:289 | ||||
chr1:54406269-54406657 | Common:10; Rare:313 | ||||
chr1:54541940-54542340 | Common:5; Rare:105 | ||||
chr1:54542360-54542870 | Common:2; Rare:117 | ||||
chr1:54715716-54715939 | Common:3; Rare:74 | ||||
chr1:54764383-54764854 | Common:14; Rare:258; Clinvar (benign):2 |