| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:97182692-97182842 | Common:2; Rare:34 | ||||
| chr5:97183172-97183556 | Common:4; Rare:145 | ||||
| chr5:98769472-98769768 | Common:2; Rare:71 | ||||
| chr5:98773435-98773697 | Common:7; Rare:69 | ||||
| chr5:98928899-98929192 | Common:4; Rare:127 | ||||
| chr5:100535209-100535424 | Rare:54 | ||||
| chr5:100903213-100903394 | Rare:35 | ||||
| chr5:102755020-102755333 | Common:3; Rare:103 | ||||
| chr5:103120111-103120404 | Common:1; Rare:70 | ||||
| chr5:103562739-103562897 | Common:7; Rare:62 | ||||
| chr5:108748673-108748982 | Common:2; Rare:106 | ||||
| chr5:109409852-109410225 | Common:4; Rare:146 | ||||
| chr5:109689246-109689438 | Common:4; Rare:92 | ||||
| chr5:110738913-110739072 | Common:2; Rare:56 | ||||
| chr5:111092238-111092402 | Common:2; Rare:90; Clinvar (benign):4 |