| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:119366749-119367059 | Common:1; Rare:94 | ||||
| chr2:119678960-119679222 | Common:5; Rare:71 | ||||
| chr2:119759790-119759871 | Common:1; Rare:26 | ||||
| chr2:121530596-121530884 | Common:7; Rare:119 | ||||
| chr2:121649418-121649645 | Common:2; Rare:65 | ||||
| chr2:121649927-121650138 | Rare:59 | ||||
| chr2:121736723-121737105 | Common:4; Rare:154 | ||||
| chr2:127294086-127294196 | Common:2; Rare:43; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:127387915-127388217 | Common:6; Rare:135 | ||||
| chr2:127811121-127811258 | Rare:45 | ||||
| chr2:127858111-127858238 | Common:1; Rare:61 | ||||
| chr2:127885886-127886305 | Common:1; Rare:112 | ||||
| chr2:128091031-128091335 | Common:8; Rare:102 | ||||
| chr2:130181553-130181780 | Common:3; Rare:100 | ||||
| chr2:130342121-130342218 | Rare:42; Clinvar:1 |