| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:173370696-173370976 | Common:2; Rare:71 | ||||
| chr4:174283631-174283946 | Common:1; Rare:58 | ||||
| chr4:177442375-177442519 | Rare:87; Clinvar:2 | ||||
| chr4:182917289-182917554 | Common:4; Rare:86 | ||||
| chr4:183504512-183504659 | Rare:54 | ||||
| chr4:184474438-184474808 | Common:1; Rare:78 | ||||
| chr4:184649403-184649756 | Common:4; Rare:119 | ||||
| chr4:184734073-184734405 | Common:5; Rare:110 | ||||
| chr4:185143132-185143315 | Common:2; Rare:61; Clinvar (benign):3 | ||||
| chr4:185395895-185396080 | Rare:58 | ||||
| chr4:185396431-185396865 | Rare:146 | ||||
| chr4:185425957-185426272 | Common:2; Rare:82 | ||||
| chr4:189940613-189940993 | Common:11; Rare:135 | ||||
| chr5:218125-218311 | Common:2; Rare:65; Clinvar:1; Clinvar (benign):2 | ||||
| chr5:443074-443206 | Common:3; Rare:57 |