| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:37157180-37157430 | Common:4; Rare:44 | ||||
| chr2:37196270-37196724 | Common:15; Rare:506 | ||||
| chr2:37196942-37197342 | Common:1; Rare:135 | ||||
| chr2:37230727-37231348 | Common:4; Rare:227 | ||||
| chr2:37231470-37231800 | Common:33; Rare:856; Clinvar:4; Clinvar (benign):28 | ||||
| chr2:37323811-37324517 | Common:11; Rare:316 | ||||
| chr2:37324562-37324980 | Common:6; Rare:466 | ||||
| chr2:37325030-37325210 | Rare:39 | ||||
| chr2:37671325-37671896 | Common:15; Rare:418 | ||||
| chr2:37672010-37672340 | Common:7; Rare:113 | ||||
| chr2:37672360-37672910 | Common:21; Rare:349 | ||||
| chr2:37924950-37925709 | Common:33; Rare:997 | ||||
| chr2:38376062-38377014 | Common:5; Rare:524 | ||||
| chr2:38377182-38377601 | Common:9; Rare:552 | ||||
| chr2:38377760-38378045 | Common:3; Rare:61 |