Proximal
K562(Human) | 24566 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:89318170-89318632 | Common:36; Rare:580 | ||||
| chr9:89318600-89319130 | Common:6; Rare:472 | ||||
| chr9:90801420-90801970 | Common:12; Rare:410 | ||||
| chr9:90801874-90802274 | Common:8; Rare:153 | ||||
| chr9:91361312-91361712 | Rare:118; Clinvar:1; Clinvar (benign):2 | ||||
| chr9:91361793-91362193 | Common:7; Rare:295; Clinvar:4; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr9:91423114-91423795 | Common:7; Rare:271 | ||||
| chr9:91423750-91424150 | Common:5; Rare:415 | ||||
| chr9:91424310-91424800 | Common:3; Rare:141 | ||||
| chr9:91948156-91948670 | Common:4; Rare:124 | ||||
| chr9:91948674-91949883 | Common:26; Rare:672 | ||||
| chr9:91949836-91949997 | Common:1; Rare:47; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:91950070-91950550 | Common:12; Rare:500; Clinvar:6 | ||||
| chr9:92114862-92115729 | Common:11; Rare:521; Clinvar:7; Clinvar (benign):1 | ||||
| chr9:92293568-92294042 | Common:38; Rare:792 |
- 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