| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:34236755-34236906 | Common:2; Rare:62 | ||||
| chr6:34248981-34249293 | Common:1; Rare:77 | ||||
| chr6:34392237-34392858 | Common:1; Rare:231 | ||||
| chr6:34426010-34426135 | Common:4; Rare:63; Clinvar:1; Clinvar (benign):8 | ||||
| chr6:34696364-34696433 | Common:1; Rare:18 | ||||
| chr6:34696688-34697029 | Common:1; Rare:72 | ||||
| chr6:34757038-34757109 | Rare:13 | ||||
| chr6:34757315-34757558 | Common:1; Rare:70 | ||||
| chr6:34757897-34757929 | Rare:8 | ||||
| chr6:34791967-34792133 | Common:3; Rare:49 | ||||
| chr6:34887933-34888097 | Common:1; Rare:49 | ||||
| chr6:35259433-35259797 | Common:3; Rare:111 | ||||
| chr6:35921047-35921261 | Common:1; Rare:90 | ||||
| chr6:36442870-36443101 | Common:2; Rare:86 | ||||
| chr6:36547305-36547593 | Common:1; Rare:120 |