| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:3231700-3231809 | Rare:19 | ||||
| chr6:4021165-4021466 | Rare:126 | ||||
| chr6:5003608-5003838 | Common:6; Rare:72 | ||||
| chr6:5260674-5261661 | Common:21; Rare:308; Clinvar (benign):4 | ||||
| chr6:7389741-7390059 | Common:1; Rare:92 | ||||
| chr6:7910632-7910714 | Common:1; Rare:30 | ||||
| chr6:7910775-7910888 | Common:1; Rare:39 | ||||
| chr6:8102437-8102718 | Common:1; Rare:101 | ||||
| chr6:8435406-8435665 | Common:4; Rare:92 | ||||
| chr6:10694586-10695061 | Common:5; Rare:136 | ||||
| chr6:10722875-10723252 | Common:6; Rare:134 | ||||
| chr6:10747631-10747877 | Common:2; Rare:97 | ||||
| chr6:11094018-11094293 | Rare:86 | ||||
| chr6:11232612-11232847 | Rare:50 | ||||
| chr6:13574373-13574632 | Common:2; Rare:65 |