| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:121870406-121870651 | Common:1; Rare:59; Clinvar (benign):1 | ||||
| chr4:122732436-122732762 | Common:1; Rare:100; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:122922929-122923118 | Common:2; Rare:51 | ||||
| chr4:123398309-123398441 | Common:1; Rare:45 | ||||
| chr4:124712613-124713089 | Common:1; Rare:137 | ||||
| chr4:127782263-127782351 | Rare:26 | ||||
| chr4:127880797-127880934 | Rare:45 | ||||
| chr4:128060987-128061325 | Common:1; Rare:124 | ||||
| chr4:128287805-128287965 | Common:2; Rare:62 | ||||
| chr4:128811144-128811317 | Rare:36 | ||||
| chr4:129093468-129093736 | Common:1; Rare:79 | ||||
| chr4:133149103-133149304 | Common:2; Rare:60 | ||||
| chr4:137532358-137532659 | Common:2; Rare:50 | ||||
| chr4:138242334-138242642 | Common:1; Rare:66 | ||||
| chr4:139301301-139301562 | Common:3; Rare:81 |