Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:100742439-100742735 | Common:2; Rare:71 | ||||
chr10:100796668-100796829 | Common:2; Rare:22 | ||||
chr10:101311208-101311290 | Common:2; Rare:17 | ||||
chr10:102121360-102121523 | Rare:20 | ||||
chr10:102679747-102679945 | Rare:32 | ||||
chr10:103090639-103090894 | Common:5; Rare:66; Clinvar (benign):1 | ||||
chr10:103153314-103153395 | Rare:17 | ||||
chr10:103192342-103192638 | Rare:68 | ||||
chr10:103659967-103660188 | Common:2; Rare:45 | ||||
chr10:103661710-103662033 | Common:1; Rare:83 | ||||
chr10:103668701-103668788 | Rare:27 | ||||
chr10:114515696-114515784 | Rare:20 | ||||
chr10:117486672-117486776 | Rare:19 | ||||
chr10:117547876-117548093 | Common:4; Rare:38 | ||||
chr10:124733221-124733437 | Rare:45 |