Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:102798058-102798196 | Common:1; Rare:42 | ||||
chr11:102798200-102798265 | Rare:14 | ||||
chr11:103092056-103092259 | Common:1; Rare:66 | ||||
chr11:105045190-105045406 | Rare:65 | ||||
chr11:106022216-106022442 | Common:2; Rare:74 | ||||
chr11:106077319-106077711 | Common:2; Rare:117 | ||||
chr11:107859186-107859293 | Rare:24 | ||||
chr11:108009273-108009349 | Rare:38 | ||||
chr11:108121429-108121675 | Common:4; Rare:91; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr11:108222575-108223043 | Rare:157; Clinvar:7 | ||||
chr11:108929328-108929667 | Common:1; Rare:58 | ||||
chr11:110092862-110093121 | Common:3; Rare:90 | ||||
chr11:110296560-110296784 | Rare:120; Clinvar:6 | ||||
chr11:111766348-111766424 | Rare:39 | ||||
chr11:111878815-111878981 | Common:2; Rare:51 |