Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:94418226-94418481 | Common:2; Rare:89 | ||||
chr1:94541743-94541991 | Rare:73 | ||||
chr1:94820222-94820422 | Common:2; Rare:53 | ||||
chr1:94926842-94927228 | Common:4; Rare:117 | ||||
chr1:95072870-95073018 | Rare:57 | ||||
chr1:95233924-95234256 | Common:5; Rare:103 | ||||
chr1:98661598-98661869 | Common:2; Rare:96 | ||||
chr1:99645957-99646342 | Rare:76 | ||||
chr1:99850309-99850662 | Rare:81; Clinvar:2; Clinvar (benign):2 | ||||
chr1:99969943-99970089 | Rare:40 | ||||
chr1:100038006-100038178 | Common:1; Rare:68 | ||||
chr1:100132979-100133210 | Rare:82 | ||||
chr1:100266107-100266419 | Common:4; Rare:111 | ||||
chr1:100352175-100352533 | Common:1; Rare:85 | ||||
chr1:100894766-100894914 | Common:1; Rare:34 |