| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:179562703-179563002 | Rare:94 | ||||
| chr3:179604632-179604921 | Common:3; Rare:110 | ||||
| chr3:180602054-180602398 | Common:1; Rare:123 | ||||
| chr3:180679487-180679544 | Rare:7; Clinvar:2 | ||||
| chr3:180989620-180989823 | Rare:88; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:182793353-182793630 | Common:3; Rare:71 | ||||
| chr3:182985903-182986022 | Common:1; Rare:26 | ||||
| chr3:183635587-183635682 | Rare:34 | ||||
| chr3:183697718-183697921 | Common:1; Rare:92 | ||||
| chr3:183884828-183884959 | Rare:56 | ||||
| chr3:184135252-184135400 | Common:2; Rare:41; Clinvar:2 | ||||
| chr3:184185880-184186208 | Common:4; Rare:119 | ||||
| chr3:184248868-184248997 | Rare:74; Clinvar:5; Clinvar (benign):2 | ||||
| chr3:184249518-184249771 | Common:1; Rare:81 | ||||
| chr3:184298979-184299276 | Common:2; Rare:86 |