Proximal
cerebellum(Human) | 8337 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:5260679-5261055 | Common:5; Rare:134; Clinvar (benign):4 | ||||
| chr6:5261275-5261591 | Common:9; Rare:87 | ||||
| chr6:6002927-6002965 | Common:1; Rare:9 | ||||
| chr6:6003375-6003603 | Rare:63 | ||||
| chr6:6006712-6007102 | Common:3; Rare:87 | ||||
| chr6:6007497-6007683 | Common:3; Rare:65 | ||||
| chr6:6588617-6588789 | Common:1; Rare:55 | ||||
| chr6:7313127-7313383 | Common:4; Rare:93 | ||||
| chr6:7389740-7389976 | Common:1; Rare:61 | ||||
| chr6:8102502-8102712 | Common:1; Rare:72 | ||||
| chr6:8435361-8435678 | Common:5; Rare:115 | ||||
| chr6:10412146-10412305 | Rare:56 | ||||
| chr6:10555815-10556000 | Rare:42; Clinvar:2 | ||||
| chr6:10556091-10556368 | Common:1; Rare:54; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:10556902-10557319 | Common:1; Rare:153; Clinvar:5; 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