| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:97663992-97664289 | Rare:85 | ||||
| chr2:98608416-98608644 | Common:1; Rare:99; Clinvar (benign):1 | ||||
| chr2:99154890-99155031 | Common:1; Rare:57 | ||||
| chr2:99180984-99181226 | Common:2; Rare:71 | ||||
| chr2:105337267-105337578 | Common:5; Rare:108 | ||||
| chr2:108534175-108534498 | Common:7; Rare:129 | ||||
| chr2:111884174-111884231 | Rare:10 | ||||
| chr2:112584393-112584633 | Common:1; Rare:65 | ||||
| chr2:113627079-113627294 | Common:2; Rare:62 | ||||
| chr2:113756577-113756776 | Common:3; Rare:70 | ||||
| chr2:119366795-119367023 | Common:1; Rare:59 | ||||
| chr2:119759785-119759922 | Common:1; Rare:42 | ||||
| chr2:121649448-121649674 | Common:2; Rare:70 | ||||
| chr2:121736867-121737103 | Common:4; Rare:75 | ||||
| chr2:121755421-121755747 | Common:2; Rare:108 |