| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:29268878-29269105 | Common:2; Rare:62 | ||||
| chr22:29388068-29388216 | Rare:39 | ||||
| chr22:29388439-29388761 | Rare:101 | ||||
| chr22:29553343-29553366 | Rare:6 | ||||
| chr22:29553613-29554001 | Common:3; Rare:127 | ||||
| chr22:29581021-29581301 | Common:3; Rare:85 | ||||
| chr22:29603140-29603740 | Common:5; Rare:138; Clinvar:3 | ||||
| chr22:29603981-29604095 | Rare:32; Clinvar:1; Clinvar (benign):2 | ||||
| chr22:29604116-29604208 | Rare:25; Clinvar (benign):1 | ||||
| chr22:29766265-29766496 | Rare:42 | ||||
| chr22:29766792-29767029 | Common:1; Rare:57 | ||||
| chr22:29767038-29767465 | Common:4; Rare:142 | ||||
| chr22:29838127-29838555 | Common:5; Rare:131 | ||||
| chr22:29882885-29883298 | Common:3; Rare:108 | ||||
| chr22:29883396-29883477 | Rare:14 |