Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:70086269-70086473 | Common:4; Rare:81 | ||||
chr2:87455346-87455625 | Common:2; Rare:55 | ||||
chr2:88016548-88016822 | Common:8; Rare:111 | ||||
chr2:91659902-91660021 | Rare:18 | ||||
chr2:95525809-95525980 | Common:1; Rare:32 | ||||
chr2:95526681-95526923 | Common:1; Rare:79 | ||||
chr2:104851448-104851681 | Rare:32 | ||||
chr2:104853204-104853363 | Common:2; Rare:32 | ||||
chr2:104853727-104854284 | Common:3; Rare:165 | ||||
chr2:105361313-105361569 | Common:2; Rare:56; Clinvar:1; Clinvar (benign):3 | ||||
chr2:108593683-108593911 | Rare:38 | ||||
chr2:113583983-113584118 | Rare:30 | ||||
chr2:131682396-131682567 | Common:4; Rare:53 | ||||
chr2:135125570-135125825 | Rare:47 | ||||
chr2:150495986-150496334 | Common:3; Rare:43 |