| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:17011816-17012216 | Common:5; Rare:230; Clinvar:4 | ||||
| chr1:17053930-17054411 | Common:18; Rare:711; Clinvar:86; Clinvar (benign):61; Clinvar (pathogenic):1 | ||||
| chr1:17248816-17249216 | Common:2; Rare:136 | ||||
| chr1:17437498-17438209 | Common:3; Rare:286 | ||||
| chr1:17438258-17438833 | Common:33; Rare:947 | ||||
| chr1:17439015-17439534 | Common:5; Rare:192 | ||||
| chr1:17439606-17440312 | Rare:774 | ||||
| chr1:18902130-18902550 | Common:5; Rare:107; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr1:18902516-18903390 | Common:43; Rare:763; Clinvar:29 | ||||
| chr1:18956576-18956976 | Common:7; Rare:259 | ||||
| chr1:19081226-19082101 | Common:11; Rare:355 | ||||
| chr1:19209503-19209912 | Common:2; Rare:146 | ||||
| chr1:19209930-19210160 | Rare:62 | ||||
| chr1:19210075-19210660 | Common:7; Rare:943 | ||||
| chr1:19240110-19240560 | Common:3; Rare:111; Clinvar (benign):1 |