| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:11012160-11012460 | Common:1; Rare:74 | ||||
| chr1:11047198-11047336 | Rare:33 | ||||
| chr1:11059887-11060379 | Common:6; Rare:277 | ||||
| chr1:11099800-11100006 | Common:4; Rare:121 | ||||
| chr1:11262472-11262846 | Common:4; Rare:214 | ||||
| chr1:11272883-11273322 | Common:2; Rare:231; Clinvar:2; Clinvar (benign):2 | ||||
| chr1:11273430-11273532 | Common:1; Rare:36; Clinvar:1; Clinvar (benign):1 | ||||
| chr1:11653310-11653596 | Common:4; Rare:95 | ||||
| chr1:11654331-11654561 | Rare:94 | ||||
| chr1:11654624-11654931 | Common:8; Rare:156 | ||||
| chr1:11805885-11806324 | Common:4; Rare:245; Clinvar:3 | ||||
| chr1:11926368-11926640 | Common:12; Rare:138 | ||||
| chr1:11934457-11934838 | Common:12; Rare:213; Clinvar:13; Clinvar (benign):2 | ||||
| chr1:11979950-11980465 | Common:7; Rare:162; Clinvar:1; Clinvar (benign):4 | ||||
| chr1:12019238-12019597 | Common:10; Rare:236 |