| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:112275994-112276345 | Rare:106 | ||||
| chr2:112481958-112482190 | Common:1; Rare:82 | ||||
| chr2:112542100-112542253 | Rare:80 | ||||
| chr2:112542314-112542495 | Common:1; Rare:77 | ||||
| chr2:112583737-112584165 | Common:2; Rare:182 | ||||
| chr2:112584263-112584656 | Common:2; Rare:111 | ||||
| chr2:112645265-112645396 | Rare:34 | ||||
| chr2:112645665-112645952 | Common:2; Rare:103 | ||||
| chr2:112763898-112764340 | Common:6; Rare:215 | ||||
| chr2:112764591-112765006 | Common:7; Rare:142; Clinvar (pathogenic):1 | ||||
| chr2:113157143-113157543 | Common:5; Rare:164 | ||||
| chr2:113627078-113627274 | Common:1; Rare:55 | ||||
| chr2:113756573-113756823 | Common:4; Rare:89 | ||||
| chr2:113889689-113890110 | Common:8; Rare:139 | ||||
| chr2:113890906-113891128 | Rare:47 |