| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:115262840-115262892 | Rare:26 | ||||
| chr5:115841519-115841589 | Common:1; Rare:53 | ||||
| chr5:115841818-115842024 | Common:3; Rare:68 | ||||
| chr5:116084959-116085058 | Common:3; Rare:47 | ||||
| chr5:119268596-119268821 | Common:1; Rare:64 | ||||
| chr5:121961924-121962030 | Common:1; Rare:46 | ||||
| chr5:122076974-122077240 | Common:1; Rare:57 | ||||
| chr5:122311608-122311776 | Common:3; Rare:32 | ||||
| chr5:122845516-122845621 | Common:3; Rare:40 | ||||
| chr5:126595192-126595370 | Common:4; Rare:78; Clinvar:1; Clinvar (benign):9 | ||||
| chr5:126776879-126777165 | Common:2; Rare:117; Clinvar:4; Clinvar (benign):4 | ||||
| chr5:127030503-127030768 | Common:2; Rare:63 | ||||
| chr5:127290694-127290844 | Rare:33 | ||||
| chr5:131170698-131171002 | Common:1; Rare:61; Clinvar (benign):1 | ||||
| chr5:131635177-131635422 | Common:1; Rare:92 |