| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:88663024-88663382 | Common:9; Rare:150 | ||||
| chr16:88706188-88706522 | Common:4; Rare:143 | ||||
| chr16:88811895-88812028 | Common:2; Rare:63; Clinvar (benign):1 | ||||
| chr16:88856925-88857183 | Common:4; Rare:121; Clinvar:1; Clinvar (benign):2 | ||||
| chr16:89093780-89093943 | Common:3; Rare:72 | ||||
| chr16:89217619-89217749 | Common:1; Rare:61 | ||||
| chr16:89508312-89508468 | Common:1; Rare:87; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:89560518-89560772 | Rare:116 | ||||
| chr16:89657647-89658151 | Common:4; Rare:249 | ||||
| chr16:89686574-89686704 | Common:6; Rare:59 | ||||
| chr16:89686891-89686956 | Rare:25 | ||||
| chr16:89720865-89720991 | Common:1; Rare:33 | ||||
| chr16:89816619-89816788 | Common:2; Rare:86; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:89873482-89873715 | Common:1; Rare:104 | ||||
| chr16:89923187-89923355 | Rare:64 |