Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr8:109334056-109334402 | Common:1; Rare:90 | ||||
chr8:116874641-116874935 | Common:5; Rare:132 | ||||
chr8:117520584-117520774 | Common:4; Rare:42 | ||||
chr8:118951820-118952134 | Common:1; Rare:91; Clinvar:7; Clinvar (benign):1 | ||||
chr8:119832818-119832916 | Common:1; Rare:36 | ||||
chr8:119855373-119855478 | Common:2; Rare:17 | ||||
chr8:119855845-119855955 | Common:1; Rare:27 | ||||
chr8:119873564-119873833 | Common:2; Rare:75 | ||||
chr8:120445075-120445429 | Common:1; Rare:89 | ||||
chr8:124474936-124475099 | Rare:48 | ||||
chr8:124539034-124539198 | Common:2; Rare:92; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr8:125091710-125091931 | Common:2; Rare:78; Clinvar (benign):3 | ||||
chr8:127735886-127736092 | Rare:47 | ||||
chr8:127736113-127736269 | Common:3; Rare:31 | ||||
chr8:133571849-133572257 | Rare:109 |