| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:118014006-118014243 | Common:2; Rare:124 | ||||
| chr2:118088124-118088540 | Common:2; Rare:109 | ||||
| chr2:119223671-119223875 | Rare:62 | ||||
| chr2:119366795-119367090 | Common:1; Rare:89 | ||||
| chr2:119431601-119431905 | Common:9; Rare:76 | ||||
| chr2:119679007-119679234 | Common:4; Rare:63 | ||||
| chr2:119759790-119759839 | Common:1; Rare:15 | ||||
| chr2:119760095-119760215 | Common:1; Rare:22 | ||||
| chr2:120012964-120013154 | Common:2; Rare:89 | ||||
| chr2:121530574-121530880 | Common:7; Rare:125 | ||||
| chr2:121649424-121649666 | Common:2; Rare:70 | ||||
| chr2:121649886-121650106 | Common:1; Rare:54 | ||||
| chr2:121736737-121737094 | Common:4; Rare:145 | ||||
| chr2:121755415-121755788 | Common:5; Rare:123 | ||||
| chr2:127294092-127294212 | Common:2; Rare:49; Clinvar:1; Clinvar (benign):2 |