Variant report

Variant rs10899311
Chromosome Location chr11:76629991-76629992
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:42 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:76597000-76631000 Weak transcription Breast Myoepithelial Primary Cells Breast
2 chr11:76613600-76631200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
3 chr11:76615600-76631200 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
4 chr11:76617800-76630000 Weak transcription Primary monocytes fromperipheralblood blood
5 chr11:76617800-76630000 Weak transcription Cortex derived primary cultured neurospheres brain
6 chr11:76618200-76637600 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr11:76618600-76630000 Weak transcription Monocytes-CD14+_RO01746 blood
8 chr11:76622600-76630000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr11:76622600-76631200 Weak transcription Spleen Spleen
10 chr11:76622800-76631200 Weak transcription HUES6 Cell Line embryonic stem cell
11 chr11:76623000-76630000 Weak transcription iPS-20b Cell Line embryonic stem cell
12 chr11:76626600-76631200 Weak transcription Esophagus oesophagus
13 chr11:76627400-76631600 Enhancers K562 blood
14 chr11:76627800-76630000 Weak transcription Primary T cells from cord blood blood
15 chr11:76628000-76630000 Weak transcription Liver Liver
16 chr11:76628000-76637600 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
17 chr11:76628200-76630000 Weak transcription Stomach Mucosa stomach
18 chr11:76628400-76630800 Weak transcription Fetal Intestine Small intestine
19 chr11:76628400-76630800 Weak transcription HepG2 liver
20 chr11:76629000-76631400 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
21 chr11:76629200-76630000 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
22 chr11:76629400-76630000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
23 chr11:76629400-76630600 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
24 chr11:76629400-76631600 Enhancers Brain Substantia Nigra brain
25 chr11:76629800-76630000 Flanking Active TSS Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
26 chr11:76629800-76630000 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
27 chr11:76629800-76630000 Enhancers Primary B cells from cord blood blood
28 chr11:76629800-76630000 Flanking Active TSS Brain Anterior Caudate brain
29 chr11:76629800-76630000 Enhancers A549 lung
30 chr11:76629800-76630000 Enhancers HMEC breast
31 chr11:76629800-76630000 Flanking Active TSS NHDF-Ad bronchial
32 chr11:76629800-76630000 Active TSS NHEK skin
33 chr11:76629800-76630000 Enhancers Osteobl bone
34 chr11:76629800-76630200 Enhancers Brain Angular Gyrus brain
35 chr11:76629800-76630200 Active TSS Brain Cingulate Gyrus brain
36 chr11:76629800-76630200 Active TSS Brain Inferior Temporal Lobe brain
37 chr11:76629800-76630200 Enhancers Fetal Intestine Large intestine
38 chr11:76629800-76630200 Active TSS Pancreatic Islets Pancreatic Islet
39 chr11:76629800-76630400 Flanking Active TSS Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
40 chr11:76629800-76630400 Enhancers Fetal Stomach stomach
41 chr11:76629800-76631400 Enhancers HUVEC blood vessel
42 chr11:76629800-76631600 Enhancers Adipose Nuclei Adipose

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