Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:3061337-3061696 | Common:3; Rare:103 | ||||
chr19:3359329-3359674 | Common:2; Rare:111 | ||||
chr19:3977576-3978016 | Common:1; Rare:157; Clinvar:1; Clinvar (benign):1 | ||||
chr19:3982782-3983313 | Common:7; Rare:201; Clinvar:1; Clinvar (benign):6 | ||||
chr19:4007463-4007775 | Common:3; Rare:113 | ||||
chr19:4182524-4182713 | Common:1; Rare:68 | ||||
chr19:4471967-4472333 | Common:6; Rare:137 | ||||
chr19:4518469-4518726 | Common:4; Rare:66 | ||||
chr19:4723755-4724078 | Common:7; Rare:128 | ||||
chr19:4867621-4867895 | Common:4; Rare:79 | ||||
chr19:4909402-4909501 | Rare:27 | ||||
chr19:5292765-5292941 | Rare:62 | ||||
chr19:5293204-5293425 | Common:1; Rare:99 | ||||
chr19:5622701-5623384 | Common:6; Rare:262 | ||||
chr19:5680488-5680772 | Rare:83 |