Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:28799600-28799623 | Rare:3 | ||||
chr22:30922240-30922319 | Rare:33 | ||||
chr22:36288727-36289301 | Common:2; Rare:174; Clinvar:6; Clinvar (benign):10 | ||||
chr22:36323234-36323526 | Common:3; Rare:50 | ||||
chr22:36331186-36331238 | Rare:8 | ||||
chr22:36331299-36331461 | Rare:37 | ||||
chr22:36331610-36331749 | Common:2; Rare:27 | ||||
chr22:36455083-36455389 | Common:4; Rare:91 | ||||
chr22:36462231-36462398 | Common:1; Rare:28 | ||||
chr22:38336179-38336291 | Rare:31 | ||||
chr22:38741011-38741228 | Rare:44 | ||||
chr22:39521525-39521792 | Common:1; Rare:130 | ||||
chr22:41653380-41653604 | Rare:48 | ||||
chr22:42938648-42938671 | Rare:9 | ||||
chr22:46043913-46043936 | Rare:8 |