| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:99315896-99316304 | Rare:130 | ||||
| chr4:104907185-104907344 | Common:1; Rare:29 | ||||
| chr4:104907356-104907413 | Rare:11 | ||||
| chr4:110476736-110476930 | Common:1; Rare:75 | ||||
| chr4:118279110-118279194 | Common:3; Rare:23 | ||||
| chr4:119454554-119454898 | Common:15; Rare:115 | ||||
| chr4:121669602-121670013 | Common:3; Rare:107 | ||||
| chr4:125314793-125314956 | Common:2; Rare:41 | ||||
| chr4:147617972-147618008 | Rare:4 | ||||
| chr4:147637145-147637205 | Rare:14 | ||||
| chr4:153684135-153684299 | Common:1; Rare:55 | ||||
| chr4:154560245-154560529 | Common:3; Rare:57 | ||||
| chr4:154565033-154565243 | Common:3; Rare:35 | ||||
| chr4:154571213-154572131 | Common:5; Rare:180; Clinvar:4; Clinvar (benign):4 | ||||
| chr4:154572133-154572586 | Common:4; Rare:89; Clinvar:5; Clinvar (benign):3 |