Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr8:144792348-144792576 | Common:2; Rare:89 | ||||
chr8:144853021-144853066 | Rare:16 | ||||
chr9:1050122-1050357 | Common:1; Rare:102 | ||||
chr9:2844047-2844320 | Common:5; Rare:102 | ||||
chr9:4679437-4679746 | Common:1; Rare:136 | ||||
chr9:4741083-4741381 | Common:5; Rare:140 | ||||
chr9:5437813-5438019 | Common:1; Rare:69 | ||||
chr9:6757865-6758087 | Common:5; Rare:83 | ||||
chr9:18473954-18474130 | Rare:45 | ||||
chr9:19102887-19103030 | Common:1; Rare:55 | ||||
chr9:21802540-21802677 | Rare:37; Clinvar:1; Clinvar (benign):1 | ||||
chr9:26892346-26892449 | Rare:44 | ||||
chr9:26947151-26947273 | Rare:43 | ||||
chr9:26956295-26956459 | Common:2; Rare:59 | ||||
chr9:33001539-33001746 | Common:3; Rare:104; Clinvar (benign):4 |