| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:124558361-124558502 | Common:2; Rare:23 | ||||
| chr8:124564772-124565048 | Common:3; Rare:46 | ||||
| chr8:125091747-125091923 | Common:1; Rare:58 | ||||
| chr8:127735231-127735532 | Rare:51 | ||||
| chr8:127735884-127736102 | Rare:47 | ||||
| chr8:127736218-127736621 | Common:3; Rare:122 | ||||
| chr8:130016376-130016757 | Common:3; Rare:109 | ||||
| chr8:132760618-132760737 | Rare:19 | ||||
| chr8:133060287-133060354 | Rare:18 | ||||
| chr8:133297154-133297676 | Common:4; Rare:184; Clinvar:4; Clinvar (benign):1 | ||||
| chr8:133499287-133499535 | Common:3; Rare:41 | ||||
| chr8:133571973-133572168 | Rare:52 | ||||
| chr8:134713010-134713131 | Common:1; Rare:40 | ||||
| chr8:140511246-140511626 | Common:2; Rare:142 | ||||
| chr8:141128337-141128654 | Common:4; Rare:100 |