| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:40040265-40040923 | Common:11; Rare:456 | ||||
| chr1:40097106-40097417 | Common:3; Rare:260; Clinvar:19; Clinvar (benign):12; Clinvar (pathogenic):16 | ||||
| chr1:40097629-40097854 | Rare:66 | ||||
| chr1:40161199-40161506 | Common:2; Rare:237 | ||||
| chr1:40257560-40257820 | Common:3; Rare:85; Clinvar:1 | ||||
| chr1:40257848-40258385 | Common:12; Rare:387; Clinvar:24; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr1:40304790-40305290 | Common:20; Rare:175; Clinvar:2; Clinvar (benign):1 | ||||
| chr1:40316430-40316826 | Common:3; Rare:131 | ||||
| chr1:40373510-40373847 | Common:2; Rare:147 | ||||
| chr1:40374436-40374673 | Common:24; Rare:88 | ||||
| chr1:40449860-40450297 | Common:16; Rare:320 | ||||
| chr1:40477089-40477374 | Common:5; Rare:154 | ||||
| chr1:40508543-40508850 | Common:15; Rare:184 | ||||
| chr1:40531450-40531809 | Common:3; Rare:207 | ||||
| chr1:40665606-40665878 | Common:4; Rare:128 |