Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:96869897-96870145 | Common:2; Rare:51 | ||||
chr2:96870290-96870383 | Rare:18 | ||||
chr2:96870819-96870881 | Rare:12 | ||||
chr2:97094835-97094955 | Common:1; Rare:24 | ||||
chr2:97663864-97664043 | Common:1; Rare:69 | ||||
chr2:98444768-98445074 | Common:1; Rare:117 | ||||
chr2:98608370-98608636 | Common:1; Rare:114; Clinvar:1; Clinvar (benign):1 | ||||
chr2:99154877-99155050 | Common:1; Rare:72; Clinvar (benign):2 | ||||
chr2:99180956-99181226 | Common:2; Rare:84 | ||||
chr2:99337307-99337578 | Rare:101 | ||||
chr2:100105374-100105472 | Rare:26 | ||||
chr2:100563176-100563286 | Rare:38 | ||||
chr2:101002095-101002318 | Rare:81 | ||||
chr2:101252658-101252917 | Common:5; Rare:87 | ||||
chr2:101253029-101253201 | Common:2; Rare:62 |