Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:12617484-12617660 | Rare:28 | ||||
chr1:12618196-12618482 | Common:1; Rare:61 | ||||
chr1:13583724-13583845 | Rare:57 | ||||
chr1:13584064-13584344 | Common:2; Rare:99 | ||||
chr1:13700157-13700284 | Rare:51 | ||||
chr1:15152386-15152550 | Rare:28 | ||||
chr1:15526575-15526885 | Common:2; Rare:94 | ||||
chr1:16155877-16155935 | Rare:12 | ||||
chr1:16155962-16156027 | Rare:17; Clinvar:1 | ||||
chr1:16156047-16156122 | Rare:17; Clinvar:1 | ||||
chr1:16352324-16352695 | Common:4; Rare:163 | ||||
chr1:16952975-16953230 | Rare:54 | ||||
chr1:17053949-17054374 | Common:3; Rare:132; Clinvar:16; Clinvar (benign):12 | ||||
chr1:17439669-17439937 | Rare:88 | ||||
chr1:18902522-18902572 | Common:2; Rare:26; Clinvar:6 |