| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:102864089-102864271 | Common:3; Rare:77 | ||||
| chr8:103298725-103298944 | Common:2; Rare:53 | ||||
| chr8:103414904-103415461 | Common:6; Rare:276 | ||||
| chr8:106657568-106658029 | Common:5; Rare:125 | ||||
| chr8:108443437-108443693 | Common:4; Rare:114 | ||||
| chr8:109334067-109334402 | Common:1; Rare:86 | ||||
| chr8:119832824-119832875 | Common:1; Rare:18 | ||||
| chr8:120445092-120445445 | Common:1; Rare:88 | ||||
| chr8:122781589-122781918 | Common:3; Rare:64 | ||||
| chr8:124474778-124475099 | Common:1; Rare:100 | ||||
| chr8:124539026-124539224 | Common:2; Rare:108; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr8:124727921-124728095 | Common:1; Rare:47 | ||||
| chr8:125091731-125091910 | Common:2; Rare:61; Clinvar (benign):2 | ||||
| chr8:126558319-126558628 | Common:1; Rare:115 | ||||
| chr8:127735842-127736618 | Common:4; Rare:202 |