| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:144008242-144008436 | Rare:68 | ||||
| chr6:144008364-144008506 | Rare:58 | ||||
| chr6:144095485-144095832 | Common:11; Rare:194 | ||||
| chr6:144285115-144285642 | Common:3; Rare:142 | ||||
| chr6:145734510-145734970 | Common:5; Rare:148 | ||||
| chr6:145735187-145735400 | Common:7; Rare:130; Clinvar:21; Clinvar (benign):11 | ||||
| chr6:145735431-145735673 | Common:5; Rare:117; Clinvar:2; Clinvar (benign):8 | ||||
| chr6:145814651-145814958 | Common:2; Rare:266 | ||||
| chr6:145963999-145964121 | Common:8; Rare:48 | ||||
| chr6:145964277-145964584 | Common:1; Rare:173 | ||||
| chr6:146543471-146543852 | Common:14; Rare:230 | ||||
| chr6:147203682-147204008 | Common:2; Rare:116 | ||||
| chr6:147204450-147204840 | Common:2; Rare:138 | ||||
| chr6:148342307-148342888 | Rare:255 | ||||
| chr6:149484936-149485232 | Common:7; Rare:97 |