Proximal
K562(Human) | 24566 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:44541500-44541847 | Rare:45 | ||||
| chrX:44542733-44543270 | Common:7; Rare:434 | ||||
| chrX:44843152-44843667 | Common:4; Rare:104 | ||||
| chrX:44843764-44844164 | Common:6; Rare:79 | ||||
| chrX:44872868-44873293 | Common:3; Rare:326 | ||||
| chrX:44873606-44873844 | Rare:53; Clinvar (benign):1 | ||||
| chrX:46446577-46446979 | Common:2; Rare:68 | ||||
| chrX:46447043-46447443 | Rare:215 | ||||
| chrX:46545093-46545603 | Common:8; Rare:337; Clinvar (benign):8 | ||||
| chrX:46759030-46759310 | Common:2; Rare:63 | ||||
| chrX:46836677-46837078 | Rare:159; Clinvar:3; Clinvar (benign):1 | ||||
| chrX:46837014-46837620 | Common:2; Rare:213; Clinvar:7; Clinvar (benign):2; Clinvar (pathogenic):4 | ||||
| chrX:46912124-46912640 | Rare:350 | ||||
| chrX:47144252-47144886 | Common:21; Rare:357; Clinvar (benign):2 | ||||
| chrX:47144975-47145338 | Rare:217 |
- 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