Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:87040201-87040324 | Common:1; Rare:40 | ||||
chr7:93639995-93640247 | Common:4; Rare:61 | ||||
chr7:100094253-100094515 | Rare:92 | ||||
chr7:100335846-100336146 | Common:1; Rare:100 | ||||
chr7:101223721-101223963 | Rare:75 | ||||
chr7:101299516-101299757 | Common:4; Rare:51 | ||||
chr7:101302654-101302991 | Common:2; Rare:74 | ||||
chr7:101308198-101308341 | Common:2; Rare:44 | ||||
chr7:103316013-103316248 | Rare:55 | ||||
chr7:105013031-105013217 | Common:1; Rare:65 | ||||
chr7:109597276-109597582 | Common:12; Rare:73 | ||||
chr7:113118535-113118669 | Common:1; Rare:43 | ||||
chr7:122116631-122116959 | Rare:97; Clinvar (pathogenic):1 | ||||
chr7:122131367-122131634 | Common:2; Rare:34 | ||||
chr7:131108131-131108183 | Rare:7 |