| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:82441980-82442264 | Common:2; Rare:86 | ||||
| chr17:82600989-82601358 | Common:2; Rare:99 | ||||
| chr17:82629695-82630092 | Common:2; Rare:73 | ||||
| chr17:82859490-82859640 | Common:3; Rare:28 | ||||
| chr17:82875460-82875598 | Common:1; Rare:34 | ||||
| chr17:82883110-82883412 | Common:6; Rare:85 | ||||
| chr17:82890571-82890724 | Common:4; Rare:43 | ||||
| chr17:82891104-82891308 | Common:5; Rare:40 | ||||
| chr18:666567-667105 | Common:50; Rare:193 | ||||
| chr18:669018-669085 | Rare:21 | ||||
| chr18:2924401-2924672 | Rare:68; Clinvar:1; Clinvar (benign):1 | ||||
| chr18:3593966-3594492 | Common:3; Rare:96 | ||||
| chr18:3603453-3603745 | Common:1; Rare:50 | ||||
| chr18:4476069-4476136 | Rare:14 | ||||
| chr18:5238005-5238135 | Common:1; Rare:51 |