| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:96662915-96663031 | Rare:23 | ||||
| chr5:97183231-97183557 | Common:3; Rare:119 | ||||
| chr5:100535238-100535406 | Rare:40 | ||||
| chr5:103120116-103120311 | Common:1; Rare:42 | ||||
| chr5:110738947-110739020 | Common:1; Rare:22 | ||||
| chr5:111092233-111092410 | Common:2; Rare:98; Clinvar:1; Clinvar (benign):4 | ||||
| chr5:111512425-111512780 | Common:3; Rare:132 | ||||
| chr5:115602110-115602153 | Rare:9 | ||||
| chr5:115841790-115842016 | Common:3; Rare:74 | ||||
| chr5:122077119-122077257 | Common:1; Rare:24 | ||||
| chr5:122845532-122845621 | Common:2; Rare:32 | ||||
| chr5:127030511-127030764 | Common:2; Rare:61 | ||||
| chr5:132866467-132866678 | Common:1; Rare:65 | ||||
| chr5:133051870-133052117 | Rare:92 | ||||
| chr5:134004642-134004827 | Common:1; Rare:70 |