Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:24310330-24310578 | Rare:73 | ||||
chr2:24491164-24491282 | Common:2; Rare:43 | ||||
chr2:24814194-24814493 | Common:1; Rare:74 | ||||
chr2:25498979-25499084 | Rare:20 | ||||
chr2:25822230-25822366 | Rare:41 | ||||
chr2:26052494-26052664 | Rare:27 | ||||
chr2:26092864-26092901 | Rare:3 | ||||
chr2:26114819-26115117 | Rare:56 | ||||
chr2:26118382-26118467 | Rare:20 | ||||
chr2:26193672-26193956 | Rare:79; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr2:26724077-26724272 | Common:1; Rare:38 | ||||
chr2:27025476-27025597 | Rare:28 | ||||
chr2:27057073-27057383 | Common:4; Rare:78 | ||||
chr2:27232147-27232429 | Common:1; Rare:69 | ||||
chr2:27241159-27241394 | Rare:69; Clinvar:1 |