Proximal
stomach(Human) | 11870 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:73683396-73683668 | Common:3; Rare:124 | ||||
| chr7:73738786-73739109 | Common:2; Rare:102 | ||||
| chr7:73842491-73842689 | Common:6; Rare:31 | ||||
| chr7:74027808-74028165 | Common:2; Rare:93; Clinvar:1; Clinvar (benign):2 | ||||
| chr7:74045031-74045266 | Common:1; Rare:63; Clinvar:2; Clinvar (benign):2 | ||||
| chr7:74046145-74046217 | Rare:24 | ||||
| chr7:74052507-74052735 | Common:2; Rare:29 | ||||
| chr7:74173946-74174441 | Common:3; Rare:192 | ||||
| chr7:74254346-74254535 | Rare:87 | ||||
| chr7:74453715-74454126 | Common:1; Rare:105 | ||||
| chr7:74657459-74657802 | Common:2; Rare:97 | ||||
| chr7:74657944-74658067 | Common:1; Rare:27 | ||||
| chr7:75878805-75879101 | Common:12; Rare:109 | ||||
| chr7:75914944-75915186 | Common:2; Rare:85; Clinvar:3; Clinvar (benign):1 | ||||
| chr7:75980867-75981149 | Rare:99; Clinvar:2; 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