Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:102869514-102869825 | Common:8; Rare:81 | ||||
chr10:102918108-102918613 | Common:2; Rare:184; Clinvar:1; Clinvar (benign):2 | ||||
chr10:103193253-103193444 | Common:4; Rare:59 | ||||
chr10:103276898-103277162 | Common:1; Rare:65 | ||||
chr10:103277598-103277736 | Common:1; Rare:35 | ||||
chr10:103351049-103351260 | Common:1; Rare:73 | ||||
chr10:103367817-103368029 | Common:3; Rare:56 | ||||
chr10:103395664-103396064 | Common:2; Rare:81 | ||||
chr10:103396385-103396751 | Rare:128 | ||||
chr10:103917615-103918015 | Rare:127 | ||||
chr10:103918450-103918660 | Common:1; Rare:44 | ||||
chr10:103967013-103967177 | Common:1; Rare:44 | ||||
chr10:104121740-104122028 | Common:1; Rare:79 | ||||
chr10:104232305-104232479 | Common:1; Rare:46 | ||||
chr10:104254747-104254938 | Rare:52 |