| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:119223629-119223869 | Common:1; Rare:74 | ||||
| chr2:119366770-119367059 | Common:1; Rare:88 | ||||
| chr2:119679016-119679225 | Common:3; Rare:61 | ||||
| chr2:120252603-120252945 | Common:3; Rare:113 | ||||
| chr2:121530599-121530906 | Common:7; Rare:146; Clinvar (pathogenic):3 | ||||
| chr2:121649427-121649669 | Common:2; Rare:70 | ||||
| chr2:121649966-121650146 | Rare:51 | ||||
| chr2:121736744-121737220 | Common:5; Rare:192 | ||||
| chr2:126655966-126656268 | Common:1; Rare:80 | ||||
| chr2:127294098-127294235 | Common:2; Rare:56; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:127526411-127526596 | Common:2; Rare:67 | ||||
| chr2:127811136-127811259 | Rare:39 | ||||
| chr2:127858107-127858376 | Common:3; Rare:95 | ||||
| chr2:127885885-127885991 | Rare:28 | ||||
| chr2:128091043-128091354 | Common:8; Rare:101 |