| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:23778250-23778542 | Common:9; Rare:140 | ||||
| chr1:23800723-23800929 | Common:1; Rare:69 | ||||
| chr1:23825358-23825556 | Common:3; Rare:64; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):3 | ||||
| chr1:24556026-24556108 | Common:2; Rare:27 | ||||
| chr1:24642890-24643209 | Rare:93 | ||||
| chr1:25232442-25232657 | Rare:87 | ||||
| chr1:25247371-25247639 | Common:2; Rare:109 | ||||
| chr1:25338214-25338447 | Common:1; Rare:80 | ||||
| chr1:25448545-25448856 | Common:1; Rare:62 | ||||
| chr1:25819885-25820204 | Common:4; Rare:95 | ||||
| chr1:25859387-25859549 | Common:1; Rare:58 | ||||
| chr1:26279934-26280182 | Rare:137 | ||||
| chr1:26432111-26432414 | Common:4; Rare:82; Clinvar:2; Clinvar (benign):1 | ||||
| chr1:26472118-26472528 | Common:5; Rare:122 | ||||
| chr1:26787877-26788228 | Common:3; Rare:100; Clinvar:2; Clinvar (benign):2 |