| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:119431709-119431862 | Common:4; Rare:37 | ||||
| chr2:119759716-119759766 | Rare:13 | ||||
| chr2:119759773-119759814 | Common:1; Rare:10 | ||||
| chr2:121530579-121530889 | Common:7; Rare:132; Clinvar (pathogenic):1 | ||||
| chr2:121649412-121649721 | Common:2; Rare:91 | ||||
| chr2:121736716-121737111 | Common:4; Rare:160 | ||||
| chr2:126655173-126655461 | Common:1; Rare:66 | ||||
| chr2:127064746-127065124 | Rare:84 | ||||
| chr2:127106860-127107053 | Common:1; Rare:48; Clinvar:3; Clinvar (benign):2 | ||||
| chr2:127387891-127388255 | Common:10; Rare:159 | ||||
| chr2:127811132-127811296 | Common:1; Rare:60 | ||||
| chr2:127858107-127858219 | Common:1; Rare:56 | ||||
| chr2:127885886-127886272 | Common:1; Rare:107 | ||||
| chr2:128091004-128091354 | Common:8; Rare:122 | ||||
| chr2:130181546-130181787 | Common:3; Rare:108 |