| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:45812302-45812800 | Common:5; Rare:144 | ||||
| chr20:45813194-45813465 | Rare:69 | ||||
| chr20:45833570-45833852 | Common:4; Rare:61 | ||||
| chr20:45857320-45857634 | Common:3; Rare:89 | ||||
| chr20:45890755-45890959 | Rare:70 | ||||
| chr20:45891197-45891413 | Common:1; Rare:66; Clinvar:3; Clinvar (benign):1 | ||||
| chr20:45895617-45896026 | Common:3; Rare:75 | ||||
| chr20:45898053-45898395 | Common:3; Rare:83; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr20:45910890-45911155 | Common:4; Rare:72 | ||||
| chr20:45934341-45934726 | Common:3; Rare:165 | ||||
| chr20:45935051-45935368 | Rare:123 | ||||
| chr20:45971729-45971991 | Common:3; Rare:79 | ||||
| chr20:46362924-46363153 | Common:2; Rare:52 | ||||
| chr20:46363686-46364125 | Common:1; Rare:93 | ||||
| chr20:46364202-46364551 | Common:3; Rare:113 |