| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:1351004-1352115 | Common:16; Rare:1103; Clinvar:41; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr16:1352222-1352622 | Common:1; Rare:101 | ||||
| chr16:1378910-1379416 | Common:11; Rare:382 | ||||
| chr16:1379550-1380230 | Common:14; Rare:651 | ||||
| chr16:1413598-1413998 | Rare:112 | ||||
| chr16:1414635-1415035 | Common:17; Rare:322 | ||||
| chr16:1420650-1421374 | Common:31; Rare:923 | ||||
| chr16:1474114-1474514 | Common:6; Rare:197 | ||||
| chr16:1474957-1475295 | Common:17; Rare:358; Clinvar:4; Clinvar (benign):3 | ||||
| chr16:1492625-1493025 | Common:4; Rare:73 | ||||
| chr16:1492956-1493094 | Common:2; Rare:41 | ||||
| chr16:1493160-1493617 | Common:28; Rare:797 | ||||
| chr16:1527933-1528738 | Common:34; Rare:483 | ||||
| chr16:1610155-1611051 | Common:11; Rare:983; Clinvar:6 | ||||
| chr16:1611886-1612515 | Common:34; Rare:1283; Clinvar:12 |