Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:103562624-103563048 | Common:8; Rare:166; Clinvar (benign):5 | ||||
chr14:103715449-103715872 | Common:1; Rare:141 | ||||
chr14:104689509-104689635 | Rare:23 | ||||
chr14:105300996-105301117 | Rare:26 | ||||
chr14:105419738-105420031 | Rare:92 | ||||
chr15:22838356-22838780 | Common:3; Rare:151 | ||||
chr15:25438963-25439227 | Common:3; Rare:98 | ||||
chr15:25862500-25862531 | Rare:4 | ||||
chr15:26866554-26866761 | Common:1; Rare:37 | ||||
chr15:26866964-26867345 | Common:3; Rare:112 | ||||
chr15:29822003-29822242 | Rare:90 | ||||
chr15:30903701-30903946 | Common:1; Rare:59 | ||||
chr15:30991533-30991680 | Common:4; Rare:51 | ||||
chr15:31365869-31366141 | Common:3; Rare:74 | ||||
chr15:31870637-31870951 | Rare:100 |