Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:94420407-94420646 | Rare:63; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr7:100335856-100336146 | Common:1; Rare:96 | ||||
chr7:105013036-105013199 | Rare:60 | ||||
chr7:107986021-107986357 | Common:1; Rare:89; Clinvar:2; Clinvar (benign):2 | ||||
chr7:111413966-111414043 | Rare:15 | ||||
chr7:113118540-113118666 | Common:1; Rare:40 | ||||
chr7:130912208-130912369 | Common:1; Rare:27 | ||||
chr7:131108073-131108374 | Rare:54 | ||||
chr7:148987246-148987538 | Common:8; Rare:94 | ||||
chr7:158818660-158818758 | Rare:14 | ||||
chr7:158818849-158818921 | Common:2; Rare:11 | ||||
chr8:47480306-47480626 | Common:2; Rare:53 | ||||
chr8:47512223-47512543 | Rare:63 | ||||
chr8:47737529-47737773 | Common:2; Rare:65 | ||||
chr8:56559473-56559794 | Common:2; Rare:57 |