Proximal
K562(Human) | 24566 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:150379829-150379940 | Rare:18 | ||||
| chr7:150400208-150400361 | Common:3; Rare:49 | ||||
| chr7:150400410-150400811 | Common:2; Rare:78 | ||||
| chr7:150404378-150404884 | Common:8; Rare:157 | ||||
| chr7:150404961-150406508 | Common:11; Rare:985 | ||||
| chr7:150685390-150685876 | Common:6; Rare:209 | ||||
| chr7:150824345-150824755 | Common:5; Rare:95 | ||||
| chr7:150954661-150955688 | Common:12; Rare:251; Clinvar:2; Clinvar (benign):15; Clinvar (pathogenic):2 | ||||
| chr7:150955729-150957110 | Common:42; Rare:864 | ||||
| chr7:150978204-150978604 | Common:16; Rare:409 | ||||
| chr7:150978715-150979115 | Common:18; Rare:61 | ||||
| chr7:150992889-150993915 | Common:8; Rare:290; Clinvar:1 | ||||
| chr7:150993959-150994359 | Common:1; Rare:73 | ||||
| chr7:151008036-151008448 | Common:1; Rare:350 | ||||
| chr7:151008560-151011048 | Common:39; Rare:1979; Clinvar (benign):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