| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:37324724-37324950 | Common:1; Rare:93 | ||||
| chr2:38076149-38076288 | Rare:37 | ||||
| chr2:38875886-38876050 | Common:1; Rare:59 | ||||
| chr2:39437065-39437453 | Common:4; Rare:139 | ||||
| chr2:43595978-43596146 | Common:1; Rare:51 | ||||
| chr2:44361467-44362005 | Common:3; Rare:171 | ||||
| chr2:46617012-46617255 | Common:6; Rare:102 | ||||
| chr2:46915724-46915910 | Common:1; Rare:56; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:47176430-47176832 | Common:4; Rare:189; Clinvar (benign):5 | ||||
| chr2:48440619-48440858 | Common:8; Rare:113 | ||||
| chr2:53767549-53767858 | Common:4; Rare:105 | ||||
| chr2:53786851-53787184 | Common:1; Rare:125 | ||||
| chr2:53970788-53971152 | Common:11; Rare:131 | ||||
| chr2:55050441-55050763 | Common:4; Rare:96 | ||||
| chr2:55232249-55232385 | Common:2; Rare:31 |