Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:76761431-76761514 | Common:2; Rare:41 | ||||
chr14:77024786-77024911 | Common:1; Rare:23 | ||||
chr14:81219339-81219504 | Rare:37 | ||||
chr14:101873980-101874236 | Common:2; Rare:36 | ||||
chr14:101948051-101948374 | Common:2; Rare:96 | ||||
chr14:104815975-104816202 | Common:1; Rare:83 | ||||
chr14:105294409-105294582 | Common:1; Rare:36 | ||||
chr14:105854593-105854716 | Rare:37 | ||||
chr14:105856105-105856185 | Common:1; Rare:27; Clinvar (benign):1 | ||||
chr14:105856992-105857077 | Rare:13 | ||||
chr14:105860536-105860632 | Common:1; Rare:58 | ||||
chr14:105862069-105862394 | Common:4; Rare:137 | ||||
chr14:105863901-105864127 | Common:5; Rare:180 | ||||
chr14:105864250-105864302 | Rare:74 | ||||
chr14:105864577-105865025 | Common:8; Rare:286 |