| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:43879492-43879921 | Common:19; Rare:114 | ||||
| chr13:44435159-44435447 | Common:3; Rare:83 | ||||
| chr13:44436783-44437033 | Common:2; Rare:77 | ||||
| chr13:44989419-44989634 | Rare:89 | ||||
| chr13:45120183-45120721 | Common:5; Rare:138 | ||||
| chr13:45341040-45341655 | Common:4; Rare:273 | ||||
| chr13:45418340-45418578 | Rare:71 | ||||
| chr13:45464713-45465039 | Common:1; Rare:81 | ||||
| chr13:46052488-46052493 | Rare:1 | ||||
| chr13:46052696-46052856 | Common:2; Rare:45 | ||||
| chr13:46211760-46212041 | Common:2; Rare:83 | ||||
| chr13:46797099-46797263 | Common:2; Rare:56 | ||||
| chr13:46797281-46797362 | Rare:21 | ||||
| chr13:48000736-48000850 | Rare:26 | ||||
| chr13:48001178-48001418 | Common:1; Rare:110; Clinvar:5; Clinvar (benign):11 |