| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:16729853-16730064 | Rare:63 | ||||
| chr20:17558809-17558948 | Common:1; Rare:21 | ||||
| chr20:17569090-17569197 | Rare:24 | ||||
| chr20:17569940-17570210 | Common:3; Rare:119 | ||||
| chr20:17682193-17682562 | Common:5; Rare:113 | ||||
| chr20:17968406-17968613 | Common:4; Rare:89 | ||||
| chr20:17968784-17969141 | Common:3; Rare:124 | ||||
| chr20:17969519-17969564 | Rare:8 | ||||
| chr20:18137744-18137952 | Common:1; Rare:77 | ||||
| chr20:18288163-18288485 | Common:1; Rare:82 | ||||
| chr20:18467137-18467448 | Common:1; Rare:64 | ||||
| chr20:18507425-18507580 | Rare:41 | ||||
| chr20:18507781-18507957 | Common:1; Rare:51; Clinvar:5; Clinvar (benign):1 | ||||
| chr20:20017242-20017372 | Rare:47 | ||||
| chr20:21125783-21126113 | Common:3; Rare:112 |