Proximal
K562(Human) | 24566 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:92134300-92135248 | Common:20; Rare:790 | ||||
| chr7:92135290-92136047 | Common:2; Rare:126 | ||||
| chr7:92245218-92245790 | Common:3; Rare:422; Clinvar (benign):5 | ||||
| chr7:92245834-92246609 | Common:27; Rare:976; Clinvar:23; Clinvar (benign):20 | ||||
| chr7:92447160-92447652 | Common:9; Rare:345 | ||||
| chr7:92447894-92448294 | Common:4; Rare:111; Clinvar:1; Clinvar (benign):6 | ||||
| chr7:92527802-92527941 | Rare:29 | ||||
| chr7:92528383-92528912 | Common:29; Rare:935; Clinvar:18; Clinvar (benign):13; Clinvar (pathogenic):9 | ||||
| chr7:92589570-92589940 | Common:2; Rare:72 | ||||
| chr7:92589896-92590296 | Common:6; Rare:316 | ||||
| chr7:92590229-92590751 | Common:6; Rare:446 | ||||
| chr7:92832666-92833688 | Common:1; Rare:319 | ||||
| chr7:92833764-92834164 | Rare:121 | ||||
| chr7:92834769-92835625 | Common:7; Rare:341 | ||||
| chr7:92835575-92835939 | Rare:110 |
- 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