| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:117520584-117520788 | Common:4; Rare:47 | ||||
| chr8:118951883-118952157 | Common:1; Rare:72; Clinvar:7; Clinvar (benign):1 | ||||
| chr8:119208227-119208467 | Common:4; Rare:97 | ||||
| chr8:119832815-119832897 | Common:1; Rare:32 | ||||
| chr8:119873564-119873904 | Common:3; Rare:103 | ||||
| chr8:120124893-120125211 | Common:2; Rare:84 | ||||
| chr8:120445090-120445467 | Common:1; Rare:98 | ||||
| chr8:122781589-122781926 | Common:3; Rare:65 | ||||
| chr8:124474562-124474714 | Rare:56 | ||||
| chr8:124474987-124475099 | Rare:37 | ||||
| chr8:124539026-124539188 | Common:2; Rare:92; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr8:124728408-124728767 | Common:5; Rare:109 | ||||
| chr8:124998176-124998531 | Common:1; Rare:135 | ||||
| chr8:125091712-125091934 | Common:2; Rare:79; Clinvar (benign):3 | ||||
| chr8:126557695-126557915 | Rare:55 |