| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:5238006-5238181 | Common:1; Rare:59 | ||||
| chr18:10403761-10403950 | Common:2; Rare:40 | ||||
| chr18:51391897-51392093 | Common:3; Rare:38 | ||||
| chr18:57630177-57630332 | Common:2; Rare:45 | ||||
| chr18:76787566-76787715 | Rare:82 | ||||
| chr18:78977881-78978109 | Rare:52 | ||||
| chr18:78978839-78978953 | Common:1; Rare:45 | ||||
| chr19:4768923-4769135 | Common:2; Rare:50 | ||||
| chr19:8161253-8161449 | Common:3; Rare:38 | ||||
| chr19:11023410-11023542 | Common:1; Rare:36; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:12194902-12195096 | Common:1; Rare:73 | ||||
| chr19:14565950-14566083 | Common:1; Rare:54 | ||||
| chr19:19776378-19776626 | Common:2; Rare:70 | ||||
| chr19:21569225-21569392 | Common:6; Rare:47 | ||||
| chr19:27793338-27793498 | Common:3; Rare:40 |