Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:89643886-89644111 | Rare:45 | ||||
chr10:89701404-89701623 | Common:1; Rare:59 | ||||
chr10:91162689-91163075 | Common:3; Rare:105 | ||||
chr10:91410255-91410476 | Common:1; Rare:80 | ||||
chr10:91633039-91633253 | Common:2; Rare:67 | ||||
chr10:91798262-91798408 | Rare:49 | ||||
chr10:92290956-92291392 | Common:5; Rare:135 | ||||
chr10:92573780-92574129 | Common:2; Rare:110 | ||||
chr10:92592960-92593169 | Common:3; Rare:61 | ||||
chr10:92848362-92848546 | Rare:67 | ||||
chr10:93482203-93482334 | Common:2; Rare:41 | ||||
chr10:93482356-93482452 | Rare:21 | ||||
chr10:93702408-93702697 | Common:5; Rare:100 | ||||
chr10:93757666-93758031 | Common:1; Rare:59; Clinvar:3; Clinvar (benign):1 | ||||
chr10:93893872-93894033 | Common:1; Rare:65 |