Proximal
H1(Human) | 12287 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:92966010-92966250 | Common:1; Rare:51 | ||||
| chr8:93700431-93700665 | Common:1; Rare:89 | ||||
| chr8:93740760-93740836 | Rare:23 | ||||
| chr8:93740907-93741202 | Common:1; Rare:92 | ||||
| chr8:93916625-93917025 | Common:5; Rare:142; Clinvar:1; Clinvar (benign):1 | ||||
| chr8:94436907-94437055 | Rare:34 | ||||
| chr8:94475002-94475174 | Common:4; Rare:50 | ||||
| chr8:94553422-94553777 | Common:3; Rare:130 | ||||
| chr8:94640626-94641267 | Common:9; Rare:162 | ||||
| chr8:94641558-94641799 | Common:1; Rare:54 | ||||
| chr8:94719608-94719728 | Common:1; Rare:26 | ||||
| chr8:94719757-94720006 | Common:1; Rare:81 | ||||
| chr8:94895648-94895849 | Common:2; Rare:62 | ||||
| chr8:94949293-94949640 | Common:3; Rare:96 | ||||
| chr8:95025035-95025174 | Common:1; Rare:49; Clinvar:2; Clinvar (benign):4; 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