| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:49132934-49133107 | Rare:56; Clinvar:2 | ||||
| chr3:49166264-49166459 | Common:2; Rare:89 | ||||
| chr3:49340003-49340233 | Common:3; Rare:136 | ||||
| chr3:49358165-49358527 | Common:6; Rare:306 | ||||
| chr3:49411888-49412435 | Common:4; Rare:396 | ||||
| chr3:49429230-49429429 | Rare:95 | ||||
| chr3:49469864-49470362 | Common:3; Rare:280 | ||||
| chr3:49470370-49470780 | Common:2; Rare:200; Clinvar (benign):4 | ||||
| chr3:49554303-49554529 | Rare:150 | ||||
| chr3:49673727-49674039 | Common:10; Rare:119 | ||||
| chr3:49674191-49674412 | Common:2; Rare:162 | ||||
| chr3:49688601-49688941 | Common:6; Rare:125; Clinvar:2 | ||||
| chr3:49689451-49689672 | Common:1; Rare:128 | ||||
| chr3:49723821-49724227 | Common:18; Rare:235 | ||||
| chr3:49786475-49786793 | Common:2; Rare:188 |