Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:98773473-98773786 | Common:9; Rare:91 | ||||
chr5:100535239-100535446 | Rare:49 | ||||
chr5:103120114-103120262 | Rare:30 | ||||
chr5:108748673-108748982 | Common:2; Rare:106 | ||||
chr5:109409848-109410224 | Common:4; Rare:146 | ||||
chr5:110738871-110739046 | Common:1; Rare:56 | ||||
chr5:112921613-112921708 | Common:2; Rare:29 | ||||
chr5:115841837-115841976 | Common:2; Rare:46 | ||||
chr5:116084878-116085055 | Common:7; Rare:70 | ||||
chr5:119525149-119525257 | Common:1; Rare:23; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr5:122077119-122077249 | Common:1; Rare:23 | ||||
chr5:128083045-128083397 | Common:8; Rare:108 | ||||
chr5:132295329-132295419 | Rare:14 | ||||
chr5:132556821-132556997 | Common:1; Rare:60; Clinvar:1 | ||||
chr5:132866490-132866671 | Common:1; Rare:55 |