Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:141319112-141319216 | Rare:23 | ||||
chr5:141319414-141319670 | Common:2; Rare:41 | ||||
chr5:141431860-141432047 | Rare:55 | ||||
chr5:145858230-145858308 | Common:1; Rare:14 | ||||
chr5:146157505-146157790 | Common:1; Rare:71; Clinvar (benign):1 | ||||
chr5:149406572-149406916 | Common:1; Rare:74 | ||||
chr5:150153069-150153273 | Common:2; Rare:44 | ||||
chr5:151108199-151108508 | Rare:69 | ||||
chr5:173320950-173320971 | Rare:5 | ||||
chr5:173474871-173474991 | Rare:25 | ||||
chr5:178206579-178206887 | Common:2; Rare:89 | ||||
chr5:179622389-179622469 | Common:1; Rare:31 | ||||
chr5:180831560-180831703 | Common:2; Rare:62 | ||||
chr6:1612136-1612179 | Common:1; Rare:14 | ||||
chr6:18258035-18258341 | Common:4; Rare:83 |