| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:2571694-2572112 | Common:9; Rare:114 | ||||
| chr18:2655020-2655450 | Common:3; Rare:118 | ||||
| chr18:2655459-2655999 | Common:34; Rare:1090 | ||||
| chr18:2656193-2656593 | Common:3; Rare:127; Clinvar:3; Clinvar (benign):1 | ||||
| chr18:2846550-2847250 | Common:9; Rare:323 | ||||
| chr18:2906507-2906870 | Common:4; Rare:222 | ||||
| chr18:3012180-3012920 | Common:13; Rare:322 | ||||
| chr18:3013092-3013662 | Common:13; Rare:511 | ||||
| chr18:3219201-3219844 | Common:7; Rare:92 | ||||
| chr18:3246820-3247030 | Common:1; Rare:41 | ||||
| chr18:3246961-3247970 | Common:38; Rare:1222 | ||||
| chr18:3248193-3248943 | Common:13; Rare:212 | ||||
| chr18:3260898-3262377 | Common:56; Rare:1332 | ||||
| chr18:3262353-3262753 | Common:8; Rare:103 | ||||
| chr18:3262956-3263213 | Common:3; Rare:70 |