Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:42782876-42782992 | Rare:45 | ||||
chr17:42787718-42787865 | Common:2; Rare:54; Clinvar:2; Clinvar (benign):2 | ||||
chr17:43315647-43315920 | Common:7; Rare:117 | ||||
chr17:43368082-43368362 | Common:9; Rare:110 | ||||
chr17:43388310-43388431 | Rare:23 | ||||
chr17:43525787-43525895 | Common:1; Rare:21 | ||||
chr17:43777415-43777453 | Rare:3 | ||||
chr17:43815689-43815713 | Rare:5 | ||||
chr17:43815805-43815857 | Rare:15 | ||||
chr17:44467372-44467436 | Rare:7 | ||||
chr17:44556538-44556811 | Common:1; Rare:65 | ||||
chr17:44558998-44559454 | Common:1; Rare:116 | ||||
chr17:44560209-44560497 | Common:2; Rare:35 | ||||
chr17:44560620-44560631 | Rare:2 | ||||
chr17:44797753-44797785 | Rare:1 |