| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:11066053-11066319 | |||||
| chr22:16592777-16592934 | Rare:23 | ||||
| chr22:17007957-17008049 | Rare:39 | ||||
| chr22:17121316-17121614 | Common:1; Rare:75 | ||||
| chr22:17159136-17159409 | Common:7; Rare:134 | ||||
| chr22:17198765-17198924 | Rare:33 | ||||
| chr22:17199565-17199674 | Common:1; Rare:37 | ||||
| chr22:17628648-17628897 | Common:2; Rare:92 | ||||
| chr22:17638689-17638830 | Rare:51 | ||||
| chr22:18001406-18001553 | Common:2; Rare:56 | ||||
| chr22:18077788-18078032 | Common:5; Rare:78; Clinvar:3; Clinvar (benign):2 | ||||
| chr22:18110602-18110831 | Rare:60 | ||||
| chr22:19122362-19122687 | Common:4; Rare:86 | ||||
| chr22:19144626-19144903 | Common:5; Rare:102 | ||||
| chr22:19178462-19178524 | Common:1; Rare:14 |