| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:23799514-23799816 | Rare:73 | ||||
| chr1:23800522-23800991 | Common:2; Rare:242 | ||||
| chr1:23825373-23825504 | Common:1; Rare:51; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr1:23958910-23959340 | Common:7; Rare:134 | ||||
| chr1:23959587-23959854 | Common:5; Rare:136 | ||||
| chr1:23980239-23980525 | Rare:170 | ||||
| chr1:24143090-24143480 | Common:1; Rare:127 | ||||
| chr1:24187251-24187436 | Common:2; Rare:44 | ||||
| chr1:24413662-24413898 | Common:2; Rare:108 | ||||
| chr1:24415505-24415889 | Common:5; Rare:160 | ||||
| chr1:24502590-24503040 | Common:3; Rare:224 | ||||
| chr1:24642882-24643608 | Common:6; Rare:395 | ||||
| chr1:24745071-24745504 | Common:6; Rare:292 | ||||
| chr1:25232472-25232667 | Rare:148 | ||||
| chr1:25246840-25247230 | Common:1; Rare:175 |