| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:119678840-119679240 | Common:6; Rare:94 | ||||
| chr2:119759542-119759667 | Rare:45 | ||||
| chr2:119759692-119759954 | Common:1; Rare:75 | ||||
| chr2:119760190-119760316 | Rare:28 | ||||
| chr2:120012722-120013203 | Common:4; Rare:169 | ||||
| chr2:120252592-120252974 | Common:3; Rare:124 | ||||
| chr2:121285200-121285319 | Rare:37 | ||||
| chr2:121504978-121505155 | Rare:27 | ||||
| chr2:121530554-121530880 | Common:8; Rare:129 | ||||
| chr2:121649418-121649776 | Common:2; Rare:105 | ||||
| chr2:121649973-121650146 | Rare:49 | ||||
| chr2:121736828-121737124 | Common:5; Rare:115 | ||||
| chr2:121755426-121755821 | Common:5; Rare:129 | ||||
| chr2:127106966-127107264 | Common:1; Rare:92; Clinvar:8; Clinvar (benign):1 | ||||
| chr2:127294077-127294266 | Common:2; Rare:76; Clinvar:1; Clinvar (benign):2 |