| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:29306518-29307097 | Common:14; Rare:411 | ||||
| chr22:29307178-29307676 | Common:4; Rare:173 | ||||
| chr22:29388420-29388820 | Common:1; Rare:272 | ||||
| chr22:29479996-29480221 | Rare:53 | ||||
| chr22:29553570-29554103 | Common:19; Rare:781 | ||||
| chr22:29580967-29581367 | Common:17; Rare:358 | ||||
| chr22:29603125-29603776 | Common:24; Rare:654; Clinvar:14; Clinvar (benign):1 | ||||
| chr22:29603861-29604261 | Common:2; Rare:237; Clinvar:6; Clinvar (benign):17 | ||||
| chr22:29766374-29766509 | Rare:41 | ||||
| chr22:29766449-29767426 | Common:35; Rare:1164 | ||||
| chr22:29799159-29799559 | Common:1; Rare:92 | ||||
| chr22:29838100-29838550 | Common:19; Rare:416 | ||||
| chr22:29882890-29883270 | Common:5; Rare:172 | ||||
| chr22:29883320-29883733 | Common:7; Rare:254 | ||||
| chr22:29883648-29883956 | Common:1; Rare:117 |