Proximal
SK-N-SH(Human) | 7944 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:56106350-56106682 | Common:8; Rare:123 | ||||
| chr7:64307268-64307593 | Common:2; Rare:72 | ||||
| chr7:65006640-65006878 | Common:3; Rare:72 | ||||
| chr7:65982174-65982328 | Common:2; Rare:51; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr7:66075570-66075934 | Rare:98; Clinvar (benign):1 | ||||
| chr7:66114762-66114895 | Common:1; Rare:66 | ||||
| chr7:66115179-66115403 | Rare:53 | ||||
| chr7:66628640-66628958 | Common:2; Rare:113; Clinvar:3 | ||||
| chr7:66681969-66682216 | Common:6; Rare:108 | ||||
| chr7:66921049-66921482 | Common:1; Rare:125 | ||||
| chr7:66994213-66994474 | Common:3; Rare:82; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr7:66995289-66995322 | Common:1; Rare:12; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr7:66995332-66995373 | Rare:19 | ||||
| chr7:66996554-66996933 | Common:2; Rare:92 | ||||
| chr7:72828139-72828484 | Common:1; Rare:97 |
- 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