Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:35231044-35231169 | Rare:29 | ||||
chr22:35836435-35836562 | Rare:28 | ||||
chr22:36288868-36289135 | Common:2; Rare:75; Clinvar:1; Clinvar (benign):2 | ||||
chr22:36455024-36455457 | Common:4; Rare:130 | ||||
chr22:36524582-36524601 | Rare:2 | ||||
chr22:37061494-37061549 | Rare:24 | ||||
chr22:37803746-37803801 | Rare:10 | ||||
chr22:37805942-37806006 | Rare:31 | ||||
chr22:39521555-39521792 | Common:1; Rare:118 | ||||
chr22:40651709-40651926 | Common:3; Rare:61 | ||||
chr22:41197463-41197594 | Common:1; Rare:32 | ||||
chr22:41381194-41381406 | Common:4; Rare:71 | ||||
chr22:41413823-41414083 | Common:2; Rare:80 | ||||
chr22:41951948-41952157 | Common:3; Rare:48 | ||||
chr22:42369246-42369498 | Common:3; Rare:59 |