| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:31400790-31401070 | Common:4; Rare:41 | ||||
| chr6:31837389-31837435 | Common:1; Rare:18 | ||||
| chr6:31839549-31839666 | Common:1; Rare:54 | ||||
| chr6:31899423-31899752 | Common:2; Rare:46 | ||||
| chr6:31965629-31965932 | Common:3; Rare:79; Clinvar:3 | ||||
| chr6:32894663-32894785 | Common:1; Rare:29 | ||||
| chr6:35356527-35356760 | Common:2; Rare:51 | ||||
| chr6:39882598-39882921 | Common:5; Rare:66 | ||||
| chr6:42744570-42744878 | Common:1; Rare:58 | ||||
| chr6:43172232-43172557 | Common:1; Rare:66 | ||||
| chr6:44251744-44252073 | Common:2; Rare:127 | ||||
| chr6:49358266-49358548 | Rare:55 | ||||
| chr6:49440269-49440428 | Rare:40; Clinvar:2; Clinvar (pathogenic):6 | ||||
| chr6:52420877-52420967 | Rare:19 | ||||
| chr6:53793667-53793794 | Common:2; Rare:20 |