| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:179025606-179026097 | Common:36; Rare:583 | ||||
| chr1:179026086-179026366 | Common:3; Rare:211 | ||||
| chr1:179081510-179082796 | Common:29; Rare:1120 | ||||
| chr1:179228820-179229390 | Common:8; Rare:258 | ||||
| chr1:179229563-179230232 | Common:31; Rare:365 | ||||
| chr1:179293173-179293617 | Common:1; Rare:148 | ||||
| chr1:179293601-179293898 | Common:10; Rare:377 | ||||
| chr1:179293888-179294288 | Common:3; Rare:87 | ||||
| chr1:179365472-179366398 | Common:106; Rare:883 | ||||
| chr1:179877647-179878047 | Rare:207 | ||||
| chr1:179881720-179882462 | Common:16; Rare:534 | ||||
| chr1:179882381-179883222 | Common:12; Rare:1579; Clinvar:61; Clinvar (benign):20 | ||||
| chr1:179954043-179954854 | Common:14; Rare:659 | ||||
| chr1:179954890-179955492 | Common:4; Rare:270 | ||||
| chr1:180154320-180155042 | Common:34; Rare:1056 |