| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:35399915-35400208 | Rare:100 | ||||
| chr22:35840341-35840545 | Rare:39 | ||||
| chr22:36239500-36239683 | Rare:59 | ||||
| chr22:36328746-36328921 | Rare:39 | ||||
| chr22:36329409-36329793 | Common:1; Rare:86 | ||||
| chr22:36387863-36387929 | Rare:11 | ||||
| chr22:36387935-36388330 | Common:2; Rare:107; Clinvar:2; Clinvar (benign):1 | ||||
| chr22:36507037-36507193 | Common:3; Rare:60 | ||||
| chr22:36528883-36528989 | Rare:42 | ||||
| chr22:36529047-36529529 | Common:6; Rare:145 | ||||
| chr22:37560276-37560525 | Common:1; Rare:82 | ||||
| chr22:37608677-37609048 | Common:1; Rare:105 | ||||
| chr22:37675368-37675710 | Common:4; Rare:98 | ||||
| chr22:37676137-37676188 | Rare:4 | ||||
| chr22:37849281-37849480 | Rare:119 |