| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:47402897-47403189 | Common:1; Rare:130; Clinvar:40; Clinvar (benign):27 | ||||
| chr2:47782939-47783189 | Common:2; Rare:108; Clinvar:3; Clinvar (benign):5 | ||||
| chr2:47905489-47905836 | Common:3; Rare:168 | ||||
| chr2:48440619-48440851 | Common:8; Rare:110 | ||||
| chr2:50347529-50347944 | Common:3; Rare:100 | ||||
| chr2:51032014-51032297 | Common:1; Rare:67; Clinvar:3 | ||||
| chr2:53767559-53767867 | Common:5; Rare:106 | ||||
| chr2:53786839-53787090 | Rare:90 | ||||
| chr2:53970765-53971157 | Common:11; Rare:146 | ||||
| chr2:54115525-54115696 | Rare:62 | ||||
| chr2:54456081-54456423 | Common:1; Rare:130 | ||||
| chr2:55050313-55050373 | Rare:24 | ||||
| chr2:55050441-55050897 | Common:7; Rare:135 | ||||
| chr2:55232249-55232719 | Common:3; Rare:129 | ||||
| chr2:55269170-55269347 | Common:2; Rare:54 |