Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:44219471-44219633 | Rare:56 | ||||
chr17:44219645-44219899 | Rare:87 | ||||
chr17:44219912-44220182 | Common:5; Rare:84 | ||||
chr17:44220432-44220920 | Common:3; Rare:176 | ||||
chr17:44220999-44221502 | Common:2; Rare:156 | ||||
chr17:44222046-44222366 | Rare:70 | ||||
chr17:44324718-44325052 | Common:4; Rare:115 | ||||
chr17:44325326-44325564 | Common:3; Rare:50 | ||||
chr17:44345009-44345366 | Rare:82; Clinvar:5; Clinvar (benign):4 | ||||
chr17:44345382-44345595 | Common:1; Rare:41 | ||||
chr17:44503172-44503796 | Common:1; Rare:216 | ||||
chr17:44689628-44690001 | Common:1; Rare:122 | ||||
chr17:44708469-44708733 | Common:1; Rare:50 | ||||
chr17:44708755-44708913 | Common:3; Rare:56 | ||||
chr17:44775635-44775999 | Common:4; Rare:64 |