Proximal
stomach(Human) | 11870 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:169620820-169621056 | Rare:56 | ||||
| chr4:169660036-169660268 | Common:1; Rare:43 | ||||
| chr4:170089954-170090311 | Common:4; Rare:118 | ||||
| chr4:173168098-173168535 | Common:4; Rare:82 | ||||
| chr4:173168605-173168953 | Common:3; Rare:117 | ||||
| chr4:173169069-173169321 | Common:2; Rare:83 | ||||
| chr4:173369748-173369935 | Common:1; Rare:63 | ||||
| chr4:173370184-173370281 | Rare:23 | ||||
| chr4:173370674-173371024 | Common:2; Rare:88 | ||||
| chr4:173371172-173371415 | Common:3; Rare:82 | ||||
| chr4:173530106-173530539 | Common:3; Rare:82 | ||||
| chr4:174283127-174283378 | Rare:38 | ||||
| chr4:174283573-174283972 | Common:1; Rare:78 | ||||
| chr4:174521937-174522169 | Common:3; Rare:62; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr4:174522271-174522626 | Common:1; Rare:110; Clinvar:3; Clinvar (benign):1; 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