| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:29024804-29025051 | Rare:62 | ||||
| chr21:29073560-29073932 | Common:2; Rare:119 | ||||
| chr21:29076562-29077314 | Common:3; Rare:190 | ||||
| chr21:29077373-29077485 | Rare:31 | ||||
| chr21:29077685-29077924 | Rare:59 | ||||
| chr21:29121868-29122052 | Common:2; Rare:26 | ||||
| chr21:29130348-29130378 | Rare:4 | ||||
| chr21:29298711-29298971 | Common:2; Rare:113 | ||||
| chr21:29299045-29299195 | Rare:46 | ||||
| chr21:29300016-29300133 | Rare:29 | ||||
| chr21:29300377-29300529 | Common:1; Rare:33 | ||||
| chr21:29300533-29300971 | Rare:96 | ||||
| chr21:31559055-31559253 | Common:2; Rare:62 | ||||
| chr21:31659478-31659870 | Common:2; Rare:173; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):7 | ||||
| chr21:31731351-31731609 | Rare:75 |