| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:34146072-34146170 | Common:1; Rare:19 | ||||
| chr6:34248449-34248563 | Rare:18 | ||||
| chr6:34248958-34249279 | Common:1; Rare:74 | ||||
| chr6:34391959-34392717 | Common:3; Rare:270 | ||||
| chr6:34425984-34426167 | Common:4; Rare:79; Clinvar:1; Clinvar (benign):8 | ||||
| chr6:34514652-34514903 | Common:2; Rare:62 | ||||
| chr6:34696717-34696993 | Common:1; Rare:65 | ||||
| chr6:34757325-34757583 | Common:1; Rare:76 | ||||
| chr6:34791975-34792119 | Common:3; Rare:43 | ||||
| chr6:34887794-34888135 | Common:2; Rare:96 | ||||
| chr6:35058103-35058304 | Rare:39 | ||||
| chr6:35259378-35259778 | Common:3; Rare:128 | ||||
| chr6:35468262-35468447 | Common:3; Rare:68 | ||||
| chr6:35921042-35921266 | Common:1; Rare:92 | ||||
| chr6:36442936-36443087 | Common:2; Rare:65 |