| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:162163932-162164133 | Common:1; Rare:46 | ||||
| chr4:165327383-165327728 | Common:3; Rare:101 | ||||
| chr4:173369802-173369846 | Rare:12 | ||||
| chr4:173370681-173370957 | Common:2; Rare:68 | ||||
| chr4:174283627-174283932 | Common:1; Rare:55 | ||||
| chr4:176065714-176066004 | Common:7; Rare:89 | ||||
| chr4:177442376-177442519 | Rare:86; Clinvar:2 | ||||
| chr4:183659132-183659343 | Common:1; Rare:63 | ||||
| chr4:184649406-184649794 | Common:4; Rare:126 | ||||
| chr4:185396563-185396865 | Rare:100 | ||||
| chr4:185425922-185426267 | Common:2; Rare:96 | ||||
| chr4:186723796-186723950 | Common:3; Rare:57 | ||||
| chr4:189940592-189940964 | Common:11; Rare:124 | ||||
| chr5:218134-218352 | Common:2; Rare:83; Clinvar:2; Clinvar (benign):3 | ||||
| chr5:1799791-1799986 | Common:4; Rare:91 |