Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:138098293-138098365 | Rare:12 | ||||
chr6:138105716-138106058 | Common:5; Rare:54 | ||||
chr6:138106262-138106599 | Common:3; Rare:55 | ||||
chr6:148507861-148508079 | Common:3; Rare:39 | ||||
chr6:152992930-152993233 | Common:1; Rare:55 | ||||
chr6:158812536-158812846 | Common:1; Rare:62 | ||||
chr6:158817336-158817379 | Rare:8 | ||||
chr7:5419031-5419286 | Rare:79 | ||||
chr7:6396031-6396164 | Rare:22 | ||||
chr7:20002760-20003057 | Common:1; Rare:52 | ||||
chr7:26193252-26193720 | Rare:168; Clinvar (benign):2 | ||||
chr7:32727917-32728137 | Common:2; Rare:71 | ||||
chr7:32728742-32728953 | Common:8; Rare:67 | ||||
chr7:43617008-43617144 | Common:3; Rare:28 | ||||
chr7:43617311-43617550 | Rare:38 |