Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:12129457-12129719 | Rare:107 | ||||
chr10:12195814-12196234 | Rare:109 | ||||
chr10:13099941-13100205 | Common:2; Rare:67; Clinvar:2; Clinvar (benign):4 | ||||
chr10:14008157-14008392 | Rare:56 | ||||
chr10:14837994-14838352 | Common:2; Rare:94 | ||||
chr10:14878631-14878886 | Common:2; Rare:78 | ||||
chr10:14954023-14954153 | Rare:43 | ||||
chr10:15097319-15097378 | Common:1; Rare:25 | ||||
chr10:15860455-15860566 | Rare:34 | ||||
chr10:17228916-17229318 | Common:3; Rare:83 | ||||
chr10:17643894-17644279 | Common:2; Rare:114 | ||||
chr10:18651579-18651748 | Common:1; Rare:70 | ||||
chr10:18659277-18659603 | Common:2; Rare:106 | ||||
chr10:19816279-19816464 | Common:5; Rare:32 | ||||
chr10:21533966-21534337 | Common:3; Rare:151 |