Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:108907884-108907922 | Rare:10 | ||||
chr6:108960727-108960944 | Rare:37 | ||||
chr6:108994551-108994746 | Rare:35 | ||||
chr6:110700862-110700925 | Rare:6 | ||||
chr6:110893335-110893628 | Common:1; Rare:83 | ||||
chr6:111686230-111686259 | Common:1; Rare:3 | ||||
chr6:111700133-111700455 | Common:1; Rare:75 | ||||
chr6:111801521-111801698 | Rare:30 | ||||
chr6:112114661-112115060 | Common:5; Rare:76; Clinvar:1; Clinvar (benign):3 | ||||
chr6:113873334-113873406 | Common:1; Rare:13 | ||||
chr6:116278348-116278395 | Rare:9 | ||||
chr6:118895097-118895270 | Rare:50 | ||||
chr6:119350589-119350737 | Common:2; Rare:32 | ||||
chr6:119831002-119831193 | Common:1; Rare:34 | ||||
chr6:121437263-121437584 | Common:9; Rare:69 |