| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:113211308-113211663 | Common:5; Rare:82 | ||||
| chr3:113211669-113211769 | Common:1; Rare:22 | ||||
| chr3:113746156-113746392 | Rare:96 | ||||
| chr3:113746997-113747092 | Common:3; Rare:13 | ||||
| chr3:114056481-114056823 | Common:2; Rare:131 | ||||
| chr3:114624186-114624407 | Common:1; Rare:44 | ||||
| chr3:114624904-114625024 | Common:1; Rare:18 | ||||
| chr3:115100182-115100399 | Rare:36 | ||||
| chr3:115147229-115147642 | Common:5; Rare:110 | ||||
| chr3:119240856-119241010 | Common:1; Rare:47 | ||||
| chr3:119294492-119294685 | Rare:38; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:119463606-119463780 | Common:3; Rare:48 | ||||
| chr3:119468848-119469015 | Rare:64 | ||||
| chr3:119579364-119579565 | Common:1; Rare:48 | ||||
| chr3:119660521-119660703 | Common:2; Rare:28 |