| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:49444010-49444293 | Common:1; Rare:99 | ||||
| chr13:49585516-49585633 | Common:1; Rare:37 | ||||
| chr13:49936231-49936569 | Common:1; Rare:104 | ||||
| chr13:49996715-49997059 | Common:1; Rare:68 | ||||
| chr13:50081952-50082262 | Common:1; Rare:86 | ||||
| chr13:50909706-50910079 | Common:1; Rare:82; Clinvar:5; Clinvar (benign):1 | ||||
| chr13:51453013-51453367 | Rare:132 | ||||
| chr13:51804094-51804261 | Common:2; Rare:52 | ||||
| chr13:52012106-52012418 | Common:2; Rare:101; Clinvar:1 | ||||
| chr13:52450596-52450691 | Rare:30 | ||||
| chr13:52455329-52455501 | Common:3; Rare:57 | ||||
| chr13:52652666-52652926 | Common:3; Rare:87 | ||||
| chr13:52848634-52848759 | Common:1; Rare:35 | ||||
| chr13:57631658-57631934 | Common:3; Rare:66 | ||||
| chr13:60397169-60397380 | Common:4; Rare:78 |