Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:86500571-86500613 | Common:1; Rare:10 | ||||
chr2:88016544-88016822 | Common:8; Rare:117 | ||||
chr2:91659912-91660071 | Rare:32 | ||||
chr2:94208265-94208474 | Rare:1 | ||||
chr2:94290212-94290483 | Rare:3 | ||||
chr2:94586984-94587326 | Rare:85 | ||||
chr2:99407536-99407839 | Rare:54 | ||||
chr2:101008226-101008392 | Common:1; Rare:66 | ||||
chr2:105361306-105361628 | Common:3; Rare:72; Clinvar:2; Clinvar (benign):3 | ||||
chr2:111495019-111495184 | Rare:29 | ||||
chr2:112508623-112508657 | |||||
chr2:113541394-113541480 | Rare:21 | ||||
chr2:113584034-113584110 | Rare:17 | ||||
chr2:120343682-120343731 | Rare:11 | ||||
chr2:120867402-120867468 | Common:1; Rare:16 |