Proximal
H9(Human) | 16978 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:924860-925120 | Common:2; Rare:69 | ||||
| chr1:959241-959463 | Common:1; Rare:107 | ||||
| chr1:1000051-1000519 | Common:8; Rare:155 | ||||
| chr1:1000703-1000964 | Common:3; Rare:71 | ||||
| chr1:1001180-1001490 | Common:3; Rare:64 | ||||
| chr1:1013323-1013505 | Common:3; Rare:59 | ||||
| chr1:1019653-1019755 | Common:1; Rare:27 | ||||
| chr1:1019930-1020121 | Common:1; Rare:66 | ||||
| chr1:1115360-1116700 | Common:10; Rare:514 | ||||
| chr1:1231482-1231636 | Common:1; Rare:47 | ||||
| chr1:1231909-1232287 | Rare:137; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr1:1273819-1274079 | Common:1; Rare:95 | ||||
| chr1:1304650-1305000 | Common:2; Rare:100 | ||||
| chr1:1305558-1305958 | Common:3; Rare:168 | ||||
| chr1:1307810-1308220 | Common:1; Rare:104 |
- 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