Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:226795017-226795127 | Rare:48 | ||||
chr2:226835909-226836068 | Rare:65 | ||||
chr2:227325207-227325423 | Common:4; Rare:74 | ||||
chr2:232550555-232550719 | Rare:61 | ||||
chr2:237085761-237085976 | Common:2; Rare:80 | ||||
chr2:237487105-237487276 | Common:3; Rare:42 | ||||
chr2:240025227-240025454 | Common:2; Rare:81; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr2:240560766-240560835 | Rare:29 | ||||
chr2:240561015-240561287 | Common:3; Rare:124 | ||||
chr2:241149439-241149647 | Common:2; Rare:66 | ||||
chr2:241239696-241239949 | Common:2; Rare:91 | ||||
chr2:241315163-241315401 | Common:4; Rare:75 | ||||
chr2:241315656-241315981 | Common:5; Rare:128 | ||||
chr2:241637086-241637225 | Common:1; Rare:52 | ||||
chr2:241637566-241637709 | Common:1; Rare:82 |