| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:102607500-102607724 | Common:1; Rare:52 | ||||
| chr4:102614939-102615117 | Common:3; Rare:39 | ||||
| chr4:105192847-105193119 | Common:3; Rare:45 | ||||
| chr4:107932127-107932336 | Common:2; Rare:49; Clinvar (benign):1 | ||||
| chr4:109434449-109434472 | Rare:6 | ||||
| chr4:117926092-117926170 | Common:1; Rare:21 | ||||
| chr4:118278523-118278769 | Common:4; Rare:95 | ||||
| chr4:118591539-118591834 | Common:4; Rare:97 | ||||
| chr4:119454556-119454911 | Common:17; Rare:121 | ||||
| chr4:128844587-128844670 | Rare:12 | ||||
| chr4:139047520-139047738 | Rare:38 | ||||
| chr4:139112353-139112520 | Rare:21 | ||||
| chr4:139177885-139178142 | Rare:79 | ||||
| chr4:139762772-139763090 | Common:3; Rare:53 | ||||
| chr4:139873627-139873774 | Rare:27 |