Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:135741611-135741960 | Common:4; Rare:127 | ||||
chr2:135985404-135985932 | Common:6; Rare:185; Clinvar (benign):1 | ||||
chr2:138501664-138502002 | Common:2; Rare:119 | ||||
chr2:143129043-143129314 | Common:1; Rare:58 | ||||
chr2:144513791-144513954 | Rare:43 | ||||
chr2:144517287-144517767 | Common:6; Rare:143; Clinvar:3; Clinvar (benign):5 | ||||
chr2:144518134-144518203 | Common:1; Rare:14 | ||||
chr2:144520021-144520528 | Common:4; Rare:103; Clinvar:1; Clinvar (benign):1 | ||||
chr2:148020681-148021310 | Common:2; Rare:153; Clinvar (benign):2 | ||||
chr2:148021369-148021658 | Rare:77 | ||||
chr2:149587306-149587397 | Rare:18 | ||||
chr2:149587669-149587826 | Common:1; Rare:45; Clinvar:2 | ||||
chr2:150485382-150485509 | Rare:30 | ||||
chr2:150487071-150487272 | Common:6; Rare:44 | ||||
chr2:151289868-151289996 | Rare:20 |