Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:113969721-113969978 | Common:1; Rare:43 | ||||
chr6:116253348-116253616 | Rare:82 | ||||
chr6:122833311-122833450 | Common:4; Rare:25 | ||||
chr6:159064560-159064776 | Common:5; Rare:33 | ||||
chr6:159170026-159170191 | Common:1; Rare:36 | ||||
chr6:163191979-163192134 | Rare:21 | ||||
chr6:163411274-163411530 | Common:1; Rare:55 | ||||
chr6:164927660-164927821 | Common:3; Rare:29 | ||||
chr7:23490417-23490550 | Common:3; Rare:57 | ||||
chr7:25855129-25855335 | Rare:46 | ||||
chr7:26193252-26193676 | Rare:150; Clinvar (benign):2 | ||||
chr7:26376166-26376387 | Common:4; Rare:64 | ||||
chr7:32728742-32728984 | Common:8; Rare:78 | ||||
chr7:33803088-33803462 | Rare:68 | ||||
chr7:35186176-35186497 | Common:1; Rare:89 |