| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:28136770-28136953 | Common:1; Rare:62 | ||||
| chr6:28161701-28161792 | Common:1; Rare:19 | ||||
| chr6:29927068-29927193 | Common:12; Rare:14 | ||||
| chr6:30286121-30286318 | Rare:28 | ||||
| chr6:31462974-31463192 | Common:4; Rare:43 | ||||
| chr6:31797991-31798222 | Common:8; Rare:45 | ||||
| chr6:32894573-32894803 | Common:9; Rare:64 | ||||
| chr6:33425670-33425872 | Common:1; Rare:51; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:35213580-35213739 | Common:1; Rare:28 | ||||
| chr6:35469970-35470340 | Common:2; Rare:86 | ||||
| chr6:36484506-36484761 | Common:1; Rare:39 | ||||
| chr6:44248415-44248777 | Common:2; Rare:118 | ||||
| chr6:44249375-44249856 | Common:1; Rare:130 | ||||
| chr6:44249867-44250155 | Common:3; Rare:103 | ||||
| chr6:44251730-44252264 | Common:3; Rare:180 |