Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:113490666-113491021 | Common:2; Rare:132 | ||||
chr13:113863832-113864180 | Common:3; Rare:85 | ||||
chr13:114281519-114281644 | Common:2; Rare:66 | ||||
chr13:114281808-114282002 | Common:5; Rare:106 | ||||
chr14:20343193-20343638 | Common:12; Rare:264 | ||||
chr14:20455042-20455313 | Common:2; Rare:79 | ||||
chr14:20684417-20684650 | Common:2; Rare:40; Clinvar (benign):2 | ||||
chr14:21022079-21022443 | Rare:92 | ||||
chr14:21025677-21025806 | Rare:26 | ||||
chr14:21070192-21070375 | Common:1; Rare:51 | ||||
chr14:21476868-21477253 | Common:1; Rare:119 | ||||
chr14:22766558-22766723 | Common:1; Rare:92 | ||||
chr14:22871695-22871886 | Rare:48 | ||||
chr14:22872087-22872252 | Common:2; Rare:39 | ||||
chr14:22929357-22929609 | Rare:57 |