Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr8:108443463-108443661 | Common:3; Rare:85 | ||||
chr8:109334051-109334400 | Common:1; Rare:90 | ||||
chr8:109540108-109540188 | Common:1; Rare:13 | ||||
chr8:116766304-116766546 | Common:4; Rare:59 | ||||
chr8:116874618-116874959 | Common:6; Rare:148; Clinvar (benign):1 | ||||
chr8:117520584-117520778 | Common:4; Rare:44 | ||||
chr8:119832829-119832916 | Common:1; Rare:28 | ||||
chr8:120445087-120445445 | Common:1; Rare:89 | ||||
chr8:121641396-121641583 | Rare:32 | ||||
chr8:123241342-123241444 | Common:1; Rare:40 | ||||
chr8:124474957-124475100 | Rare:46 | ||||
chr8:124538981-124539204 | Common:2; Rare:127; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr8:125091712-125091949 | Common:2; Rare:80; Clinvar (benign):3 | ||||
chr8:127735895-127736076 | Rare:40 | ||||
chr8:127736118-127736261 | Common:3; Rare:27 |