| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:210477582-210477638 | Rare:20 | ||||
| chr2:212538533-212538690 | Rare:55 | ||||
| chr2:213284238-213284490 | Rare:82 | ||||
| chr2:215311910-215312150 | Common:8; Rare:101 | ||||
| chr2:215409568-215410031 | Rare:129 | ||||
| chr2:215436004-215436253 | Common:2; Rare:76 | ||||
| chr2:216081761-216081978 | Common:1; Rare:65 | ||||
| chr2:216082934-216083023 | Rare:12 | ||||
| chr2:216372368-216372665 | Rare:65 | ||||
| chr2:216412241-216412534 | Common:2; Rare:66; Clinvar (benign):1 | ||||
| chr2:216498744-216498894 | Common:5; Rare:64 | ||||
| chr2:216694616-216694659 | Rare:11 | ||||
| chr2:218217064-218217246 | Common:1; Rare:66 | ||||
| chr2:218270098-218270547 | Common:5; Rare:141; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:218292481-218292626 | Common:1; Rare:43 |