| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:2798829-2799079 | Common:2; Rare:51 | ||||
| chr4:2799505-2799615 | Common:1; Rare:16 | ||||
| chr4:2812202-2812381 | Rare:30 | ||||
| chr4:2812728-2812856 | Common:3; Rare:39 | ||||
| chr4:2826805-2826913 | Common:2; Rare:29 | ||||
| chr4:2843679-2844018 | Common:3; Rare:125 | ||||
| chr4:2934771-2934910 | Common:1; Rare:66 | ||||
| chr4:2963315-2963587 | Common:2; Rare:102 | ||||
| chr4:3074547-3074715 | Common:2; Rare:56 | ||||
| chr4:3369897-3370213 | Common:2; Rare:71 | ||||
| chr4:3485435-3485608 | Common:4; Rare:68; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
| chr4:3532208-3532231 | Rare:8; Clinvar (pathogenic):1 | ||||
| chr4:3532234-3532286 | Rare:19 | ||||
| chr4:4248179-4248266 | Common:3; Rare:42 | ||||
| chr4:4290038-4290307 | Common:5; Rare:101 |