Proximal
K562(Human) | 24566 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:95024729-95025457 | Common:12; Rare:829; Clinvar:6; Clinvar (benign):49; Clinvar (pathogenic):8 | ||||
| chr8:95133469-95133983 | Common:20; Rare:756 | ||||
| chr8:95134015-95134415 | Common:2; Rare:102 | ||||
| chr8:95268580-95269073 | Common:55; Rare:466; Clinvar (benign):1 | ||||
| chr8:95269060-95270123 | Common:69; Rare:1285; Clinvar:6; Clinvar (benign):2 | ||||
| chr8:96234880-96235280 | Common:2; Rare:158 | ||||
| chr8:96235293-96235766 | Common:5; Rare:562; Clinvar (benign):13 | ||||
| chr8:96261516-96261993 | Common:42; Rare:992 | ||||
| chr8:96262049-96262506 | Common:1; Rare:197 | ||||
| chr8:96644228-96645800 | Common:15; Rare:722 | ||||
| chr8:96761066-96761466 | Rare:100 | ||||
| chr8:97643649-97644549 | Common:65; Rare:1023 | ||||
| chr8:97644717-97645844 | Common:12; Rare:885 | ||||
| chr8:97775510-97776024 | Common:32; Rare:898; Clinvar (benign):2 | ||||
| chr8:98044522-98045045 | Common:5; Rare:260 |
- 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