Proximal
K562(Human) | 24566 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:73562903-73563324 | Common:3; Rare:172 | ||||
| chrX:73563380-73563620 | Rare:129 | ||||
| chrX:74614443-74614919 | Common:5; Rare:435 | ||||
| chrX:75155380-75155780 | Common:3; Rare:52 | ||||
| chrX:75156171-75156571 | Common:9; Rare:303 | ||||
| chrX:75273403-75273803 | Rare:71 | ||||
| chrX:75273851-75274251 | Rare:165 | ||||
| chrX:75274370-75274900 | Common:15; Rare:229 | ||||
| chrX:75522893-75523327 | Common:2; Rare:157; Clinvar:1 | ||||
| chrX:76172504-76173302 | Rare:251 | ||||
| chrX:76173410-76173900 | Common:2; Rare:183 | ||||
| chrX:77785351-77785751 | Common:1; Rare:39 | ||||
| chrX:77785930-77786460 | Common:6; Rare:199; Clinvar (benign):2 | ||||
| chrX:77895340-77895811 | Common:3; Rare:663; Clinvar:18; Clinvar (benign):9; Clinvar (pathogenic):9 | ||||
| chrX:77899166-77899904 | Common:4; Rare:515; Clinvar:1; Clinvar (benign):5 |
- 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