| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:50149041-50149441 | Common:1; Rare:102 | ||||
| chr22:50169990-50170410 | Common:8; Rare:225 | ||||
| chr22:50185673-50185981 | Common:5; Rare:121 | ||||
| chr22:50190413-50190670 | Common:9; Rare:201 | ||||
| chr22:50200717-50201138 | Common:15; Rare:379 | ||||
| chr22:50244400-50244720 | Common:8; Rare:266; Clinvar (benign):2 | ||||
| chr22:50244899-50245205 | Common:6; Rare:252 | ||||
| chr22:50256990-50257340 | Common:2; Rare:123 | ||||
| chr22:50261230-50261434 | Common:4; Rare:101 | ||||
| chr22:50261600-50261990 | Common:5; Rare:156 | ||||
| chr22:50269790-50270280 | Common:10; Rare:228 | ||||
| chr22:50270315-50270984 | Common:6; Rare:417 | ||||
| chr22:50282507-50282796 | Common:8; Rare:207 | ||||
| chr22:50307531-50307695 | Rare:96 | ||||
| chr22:50326850-50327287 | Common:9; Rare:343 |