Proximal
GM23248(Human) | 3434 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:69013590-69013949 | Common:2; Rare:121 | ||||
| chr3:69052216-69052470 | Common:6; Rare:90 | ||||
| chr3:72996709-72997047 | Common:2; Rare:125 | ||||
| chr3:79019440-79019503 | Common:1; Rare:19 | ||||
| chr3:81761534-81761735 | Common:8; Rare:74; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:86991098-86991322 | Common:1; Rare:60 | ||||
| chr3:87227032-87227380 | Common:2; Rare:105; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:88058923-88059325 | Common:3; Rare:152 | ||||
| chr3:88149605-88150010 | Common:1; Rare:105 | ||||
| chr3:93979927-93980190 | Common:3; Rare:92; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:94062920-94063040 | Rare:33 | ||||
| chr3:97764508-97764811 | Common:1; Rare:71; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:99876113-99876312 | Common:1; Rare:53 | ||||
| chr3:100401402-100401576 | Common:1; Rare:32 | ||||
| chr3:100492420-100492744 | Common:2; Rare:95 |
- Legend for epigenomic status:
- : Enriched for H3K27ac and DNaseI signal
- : Enriched for H3K4me3 and DNaseI signal
- : Enriched for CTCF binding signal
- Legend for core promoter element:
- : Found Initiator
- : Found DPR
- : Enriched TATA box