| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:109409866-109410025 | Common:4; Rare:76 | ||||
| chr5:110738915-110739078 | Common:2; Rare:60 | ||||
| chr5:111092231-111092402 | Common:2; Rare:95; Clinvar:1; Clinvar (benign):4 | ||||
| chr5:111757153-111757335 | Common:5; Rare:37 | ||||
| chr5:115262837-115262892 | Rare:27 | ||||
| chr5:115841533-115841591 | Common:1; Rare:40 | ||||
| chr5:115841829-115842046 | Common:4; Rare:70 | ||||
| chr5:119268600-119268837 | Common:1; Rare:65 | ||||
| chr5:119355839-119356021 | Common:2; Rare:46 | ||||
| chr5:122077109-122077257 | Common:1; Rare:25 | ||||
| chr5:122845516-122845625 | Common:3; Rare:43 | ||||
| chr5:123423317-123423625 | Rare:107 | ||||
| chr5:124748771-124748997 | Common:2; Rare:53 | ||||
| chr5:126595192-126595324 | Common:2; Rare:60; Clinvar:1; Clinvar (benign):7 | ||||
| chr5:126776880-126777184 | Common:2; Rare:120; Clinvar:4; Clinvar (benign):4 |