| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:924730-925160 | Common:8; Rare:286 | ||||
| chr1:925559-925951 | Common:4; Rare:183 | ||||
| chr1:940130-940430 | Common:7; Rare:120 | ||||
| chr1:941687-942116 | Common:5; Rare:457 | ||||
| chr1:959047-959585 | Common:11; Rare:729 | ||||
| chr1:960345-961477 | Common:21; Rare:1099 | ||||
| chr1:966241-966641 | Common:13; Rare:337 | ||||
| chr1:966841-967241 | Common:2; Rare:480 | ||||
| chr1:980630-981010 | Common:4; Rare:117 | ||||
| chr1:999513-999913 | Common:4; Rare:205 | ||||
| chr1:999952-1000557 | Common:49; Rare:966 | ||||
| chr1:1000570-1001140 | Common:20; Rare:559 | ||||
| chr1:1001193-1001593 | Common:3; Rare:80 | ||||
| chr1:1013070-1013690 | Common:25; Rare:402 | ||||
| chr1:1019248-1020436 | Common:21; Rare:947; Clinvar:7; Clinvar (benign):2 |