Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:68383430-68384330 | Common:3; Rare:217 | ||||
chr17:68391540-68391940 | Common:8; Rare:149 | ||||
chr17:68474420-68474810 | Common:3; Rare:125 | ||||
chr17:68485190-68485700 | Common:4; Rare:142 | ||||
chr17:68509067-68509962 | Common:11; Rare:261 | ||||
chr17:68522530-68522910 | Common:1; Rare:96; Clinvar:3; Clinvar (benign):10; Clinvar (pathogenic):3 | ||||
chr17:68613881-68614037 | Rare:28 | ||||
chr17:68820990-68821510 | Common:3; Rare:109 | ||||
chr17:72122758-72123158 | Common:4; Rare:221; Clinvar:6; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
chr17:72339010-72339370 | Common:2; Rare:114 | ||||
chr17:72399630-72400060 | Common:6; Rare:158 | ||||
chr17:72400222-72400440 | Common:4; Rare:63 | ||||
chr17:72403760-72404580 | Common:5; Rare:194 | ||||
chr17:72413200-72413860 | Common:3; Rare:219 | ||||
chr17:72421394-72421580 | Rare:27 |