Variant report

Variant rs386709861
Chromosome Location chr7:6928886-6928887
allele CAGAT/TGCAC
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:6927000-6930200 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
2 chr7:6927400-6929000 Enhancers Fetal Heart heart
3 chr7:6927800-6929200 Enhancers NHDF-Ad bronchial
4 chr7:6928200-6929400 Weak transcription Brain Hippocampus Middle brain
5 chr7:6928800-6929200 ZNF genes & repeats H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
6 chr7:6928800-6929200 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
7 chr7:6928800-6929200 Enhancers Esophagus oesophagus
8 chr7:6928800-6929200 ZNF genes & repeats Fetal Brain Male brain
9 chr7:6928800-6929200 Enhancers Gastric stomach
10 chr7:6928800-6929200 Enhancers Right Atrium heart
11 chr7:6928800-6929400 ZNF genes & repeats H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
12 chr7:6928800-6929400 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
13 chr7:6928800-6929400 ZNF genes & repeats iPS DF 19.11 Cell Line embryonic stem cell
14 chr7:6928800-6929400 ZNF genes & repeats Fetal Kidney kidney
15 chr7:6928800-6929400 Bivalent/Poised TSS Fetal Lung lung
16 chr7:6928800-6929400 Enhancers Pancreas Pancrea

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