| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:119300490-119300928 | Common:2; Rare:194 | ||||
| chr4:119627867-119628107 | Common:3; Rare:50 | ||||
| chr4:119628128-119628183 | Rare:9 | ||||
| chr4:120066748-120066964 | Common:4; Rare:65 | ||||
| chr4:120922687-120923005 | Common:1; Rare:89; Clinvar:4 | ||||
| chr4:121801233-121801396 | Common:2; Rare:54 | ||||
| chr4:122732436-122732776 | Common:2; Rare:102; Clinvar:2; Clinvar (benign):2 | ||||
| chr4:122922535-122922828 | Common:3; Rare:105 | ||||
| chr4:122922897-122923139 | Common:2; Rare:68 | ||||
| chr4:123399333-123399653 | Common:1; Rare:98 | ||||
| chr4:127880764-127880944 | Rare:63 | ||||
| chr4:129093451-129093736 | Common:1; Rare:81 | ||||
| chr4:133149085-133149323 | Common:2; Rare:73 | ||||
| chr4:137532358-137532631 | Common:2; Rare:48 | ||||
| chr4:139301251-139301587 | Common:4; Rare:102 |