Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:7410997-7411079 | Rare:14 | ||||
chr10:7787823-7788261 | Common:1; Rare:173 | ||||
chr10:7799572-7799908 | Common:1; Rare:81 | ||||
chr10:8053474-8053674 | Rare:59 | ||||
chr10:8054363-8054733 | Common:2; Rare:96 | ||||
chr10:12042759-12042956 | Rare:53 | ||||
chr10:12129433-12129768 | Common:1; Rare:142 | ||||
chr10:12195742-12195987 | Rare:56 | ||||
chr10:13099764-13100298 | Common:5; Rare:129; Clinvar:3; Clinvar (benign):6 | ||||
chr10:13348003-13348069 | Rare:13 | ||||
chr10:13586923-13587093 | Common:1; Rare:66 | ||||
chr10:13707171-13707403 | Common:3; Rare:43 | ||||
chr10:14604249-14604543 | Common:4; Rare:129 | ||||
chr10:14838007-14838375 | Common:2; Rare:101 | ||||
chr10:14878655-14878908 | Common:2; Rare:73 |