| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:47931534-47931861 | Common:2; Rare:104 | ||||
| chr18:48538800-48539290 | Common:6; Rare:388 | ||||
| chr18:48539528-48540750 | Common:6; Rare:533 | ||||
| chr18:48932974-48933374 | Rare:146 | ||||
| chr18:48933712-48934429 | Common:7; Rare:179 | ||||
| chr18:48948380-48948650 | Common:1; Rare:91 | ||||
| chr18:48948820-48950191 | Common:4; Rare:542 | ||||
| chr18:49460535-49460980 | Common:11; Rare:462; Clinvar:18; Clinvar (benign):5 | ||||
| chr18:49486550-49487001 | Common:3; Rare:166 | ||||
| chr18:49487100-49487680 | Common:16; Rare:575 | ||||
| chr18:49491304-49491638 | Common:1; Rare:114 | ||||
| chr18:49491565-49491965 | Common:3; Rare:324 | ||||
| chr18:49492346-49492787 | Common:4; Rare:216 | ||||
| chr18:49492806-49493206 | Common:4; Rare:109 | ||||
| chr18:49561772-49562172 | Common:1; Rare:308 |