Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr15:22757542-22757932 | Common:5; Rare:111 | ||||
chr15:23303467-23303794 | Common:1; Rare:31 | ||||
chr15:23564734-23565110 | Rare:80 | ||||
chr15:23646377-23646668 | Common:3; Rare:96; Clinvar:3; Clinvar (benign):2 | ||||
chr15:23686209-23686425 | Common:2; Rare:70; Clinvar (benign):1 | ||||
chr15:23762159-23762426 | Rare:70 | ||||
chr15:24857835-24858000 | Common:1; Rare:28 | ||||
chr15:24859020-24859190 | Common:1; Rare:33 | ||||
chr15:24956265-24956399 | Common:2; Rare:51 | ||||
chr15:24956595-24956799 | Common:4; Rare:54 | ||||
chr15:25330486-25330697 | Common:1; Rare:47 | ||||
chr15:26179001-26179213 | Rare:48 | ||||
chr15:28589187-28589521 | Common:1; Rare:10 | ||||
chr15:28590025-28590067 | Rare:11 | ||||
chr15:28985116-28985234 | Common:1; Rare:16 |