| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:105337269-105337578 | Common:5; Rare:108 | ||||
| chr2:106194288-106194568 | Common:4; Rare:106 | ||||
| chr2:108534199-108534534 | Common:8; Rare:135 | ||||
| chr2:111884179-111884255 | Rare:16 | ||||
| chr2:112055445-112055523 | Common:1; Rare:16 | ||||
| chr2:112584393-112584633 | Common:1; Rare:65 | ||||
| chr2:112645678-112645951 | Common:2; Rare:100 | ||||
| chr2:113627077-113627239 | Rare:42 | ||||
| chr2:113889777-113890320 | Common:8; Rare:161 | ||||
| chr2:119366761-119367065 | Common:1; Rare:91 | ||||
| chr2:119759785-119760160 | Common:4; Rare:99 | ||||
| chr2:121649448-121649683 | Common:2; Rare:74 | ||||
| chr2:121736851-121737103 | Common:4; Rare:87 | ||||
| chr2:127294137-127294281 | Common:2; Rare:49; Clinvar (benign):2 | ||||
| chr2:127675102-127675257 | Common:2; Rare:29 |