| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:130019193-130019540 | Common:1; Rare:105 | ||||
| chr6:130020562-130021425 | Common:6; Rare:350 | ||||
| chr6:130365320-130365710 | Common:2; Rare:100 | ||||
| chr6:130365730-130366140 | Common:4; Rare:94 | ||||
| chr6:131061814-131063058 | Common:7; Rare:455 | ||||
| chr6:131063155-131063328 | Rare:45 | ||||
| chr6:131135195-131135295 | Rare:29 | ||||
| chr6:131135510-131136010 | Common:5; Rare:172 | ||||
| chr6:131628181-131628471 | Common:2; Rare:73 | ||||
| chr6:131807835-131808021 | Common:4; Rare:45; Clinvar (benign):1 | ||||
| chr6:131951351-131951528 | Common:1; Rare:39 | ||||
| chr6:132513025-132513324 | Common:1; Rare:71 | ||||
| chr6:132798170-132798530 | Common:4; Rare:83 | ||||
| chr6:132798550-132798920 | Common:9; Rare:74 | ||||
| chr6:132814250-132814580 | Common:4; Rare:107 |