| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:88570179-88570472 | Common:1; Rare:113 | ||||
| chr16:88663078-88663371 | Common:8; Rare:120 | ||||
| chr16:88856850-88857166 | Common:4; Rare:150; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:89217619-89217743 | Common:1; Rare:58 | ||||
| chr16:89560541-89560725 | Rare:80 | ||||
| chr16:89657664-89658053 | Common:3; Rare:206 | ||||
| chr16:89720865-89721045 | Common:1; Rare:58 | ||||
| chr16:89972521-89972648 | Rare:47 | ||||
| chr17:714782-714963 | Common:3; Rare:59 | ||||
| chr17:752789-752895 | Rare:26 | ||||
| chr17:1491615-1491827 | Common:1; Rare:66 | ||||
| chr17:1516628-1516978 | Common:1; Rare:125 | ||||
| chr17:1716228-1716534 | Common:3; Rare:92 | ||||
| chr17:1776367-1776603 | Common:6; Rare:63; Clinvar:1 | ||||
| chr17:1829805-1830039 | Common:6; Rare:101 |