Proximal
HCT116(Human) | 17414 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:177403666-177404009 | Rare:98; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr5:177404482-177404621 | Common:2; Rare:44; Clinvar (benign):2 | ||||
| chr5:177425900-177426074 | Rare:45 | ||||
| chr5:177426209-177426561 | Common:3; Rare:106 | ||||
| chr5:177446491-177446849 | Common:2; Rare:100 | ||||
| chr5:177447879-177448055 | Common:2; Rare:35 | ||||
| chr5:177472866-177472985 | Rare:39 | ||||
| chr5:177473616-177473824 | Common:1; Rare:65 | ||||
| chr5:177496868-177497089 | Common:3; Rare:47 | ||||
| chr5:177497509-177497914 | Common:2; Rare:136 | ||||
| chr5:177516903-177517319 | Common:2; Rare:130; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr5:177554541-177554754 | Common:2; Rare:72 | ||||
| chr5:177592000-177592330 | Common:2; Rare:134; Clinvar:1 | ||||
| chr5:177600004-177600175 | Common:3; Rare:51 | ||||
| chr5:177604097-177604277 | Rare:76; Clinvar (benign):2; Clinvar (pathogenic):1 |
- 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