| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:109334062-109334400 | Common:1; Rare:85 | ||||
| chr8:118951875-118952149 | Common:1; Rare:71; Clinvar:7; Clinvar (benign):1 | ||||
| chr8:120445097-120445429 | Common:1; Rare:80 | ||||
| chr8:124539058-124539181 | Common:1; Rare:65; Clinvar (benign):5 | ||||
| chr8:143018393-143018563 | Common:2; Rare:51 | ||||
| chr8:143829310-143829519 | Rare:81 | ||||
| chr8:144082513-144082670 | Common:2; Rare:54 | ||||
| chr8:144792353-144792577 | Common:2; Rare:86 | ||||
| chr9:2844057-2844349 | Common:4; Rare:110 | ||||
| chr9:4679437-4679682 | Rare:112 | ||||
| chr9:19127488-19127778 | Common:6; Rare:87 | ||||
| chr9:19380192-19380354 | Common:4; Rare:80 | ||||
| chr9:21994350-21994374 | Rare:7; Clinvar:1; Clinvar (benign):3 | ||||
| chr9:26947146-26947210 | Rare:24 | ||||
| chr9:27573443-27573553 | Common:5; Rare:68 |