Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:89128393-89128474 | Common:1; Rare:27 | ||||
chr1:89302200-89302460 | Common:2; Rare:58 | ||||
chr1:89688633-89688862 | Rare:27 | ||||
chr1:89984198-89984335 | Common:2; Rare:36 | ||||
chr1:90717957-90718202 | Common:1; Rare:90 | ||||
chr1:90836095-90836218 | Rare:23 | ||||
chr1:90851006-90851154 | Common:1; Rare:29 | ||||
chr1:90851574-90851746 | Common:2; Rare:48 | ||||
chr1:91410932-91411048 | Common:1; Rare:17 | ||||
chr1:91498636-91498784 | Common:2; Rare:21 | ||||
chr1:92168664-92168930 | Common:1; Rare:47 | ||||
chr1:92837297-92837633 | Common:1; Rare:92; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr1:93009535-93009732 | Common:1; Rare:46 | ||||
chr1:93170804-93170999 | Rare:47 | ||||
chr1:93320154-93320262 | Common:1; Rare:14 |