| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:118988499-118988749 | Common:1; Rare:92 | ||||
| chr5:119070826-119071182 | Common:4; Rare:109 | ||||
| chr5:119071304-119071567 | Common:1; Rare:96 | ||||
| chr5:119268579-119268846 | Common:1; Rare:72 | ||||
| chr5:119355790-119355960 | Common:1; Rare:55 | ||||
| chr5:119452336-119452817 | Common:1; Rare:201; Clinvar:5; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr5:121961708-121962087 | Common:15; Rare:144 | ||||
| chr5:122312194-122312241 | Rare:18 | ||||
| chr5:122845323-122845472 | Rare:42 | ||||
| chr5:122845516-122845693 | Common:3; Rare:67 | ||||
| chr5:123423301-123423627 | Common:1; Rare:115 | ||||
| chr5:123511952-123512391 | Common:2; Rare:125 | ||||
| chr5:123512429-123512569 | Rare:39 | ||||
| chr5:123512612-123512694 | Common:1; Rare:28 | ||||
| chr5:124746589-124746809 | Common:1; Rare:45 |