Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr8:127794372-127794548 | Rare:46 | ||||
chr8:140688738-140688997 | Common:1; Rare:50 | ||||
chr8:143281636-143281925 | Common:3; Rare:63 | ||||
chr8:143300931-143301025 | Rare:15 | ||||
chr8:143816772-143816873 | Rare:42 | ||||
chr8:143929139-143929391 | Common:2; Rare:107; Clinvar:9; Clinvar (benign):5 | ||||
chr8:143935111-143935316 | Common:1; Rare:77; Clinvar:5; Clinvar (benign):4 | ||||
chr8:143977993-143978225 | Rare:55 | ||||
chr8:144105722-144105996 | Common:2; Rare:86; Clinvar (benign):1 | ||||
chr8:144619025-144619279 | Common:1; Rare:59 | ||||
chr8:145002825-145003045 | Common:2; Rare:79 | ||||
chr9:686454-686802 | Common:4; Rare:87 | ||||
chr9:693402-693714 | Common:1; Rare:72 | ||||
chr9:14993186-14993330 | Common:3; Rare:49 | ||||
chr9:15479622-15479778 | Common:1; Rare:52 |