| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:63422260-63422345 | Rare:25 | ||||
| chr18:63969754-63970133 | Common:2; Rare:65 | ||||
| chr18:68714948-68715359 | Common:8; Rare:166 | ||||
| chr18:70205638-70205803 | Common:3; Rare:70; Clinvar (benign):2 | ||||
| chr18:70205962-70206067 | Rare:40 | ||||
| chr18:74291850-74292003 | Rare:57; Clinvar:1 | ||||
| chr18:74597611-74597910 | Common:2; Rare:79 | ||||
| chr18:76822265-76822640 | Common:11; Rare:102 | ||||
| chr18:79069218-79069421 | Common:2; Rare:64 | ||||
| chr18:79343883-79344187 | Common:3; Rare:57 | ||||
| chr18:79679276-79679587 | Common:1; Rare:154 | ||||
| chr18:79679768-79679872 | Common:1; Rare:24 | ||||
| chr18:79988520-79988621 | Common:1; Rare:44 | ||||
| chr19:291030-291464 | Common:3; Rare:151 | ||||
| chr19:571490-571533 | Common:1; Rare:16 |