Variant report

Variant rs7111647
Chromosome Location chr11:10205396-10205397
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:10178200-10213400 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
2 chr11:10184600-10211400 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
3 chr11:10186200-10209200 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
4 chr11:10188000-10222800 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
5 chr11:10194800-10206800 Weak transcription Cortex derived primary cultured neurospheres brain
6 chr11:10202400-10216000 Weak transcription Fetal Intestine Small intestine
7 chr11:10203400-10208600 Weak transcription Breast Myoepithelial Primary Cells Breast
8 chr11:10203600-10215600 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
9 chr11:10203600-10220000 Weak transcription NH-A brain
10 chr11:10203800-10207000 Weak transcription Fetal Lung lung
11 chr11:10203800-10223800 Weak transcription Fetal Adrenal Gland Adrenal Gland
12 chr11:10204400-10208800 Weak transcription Ovary ovary
13 chr11:10204400-10217200 Weak transcription Fetal Intestine Large intestine
14 chr11:10204600-10211000 Weak transcription Fetal Heart heart
15 chr11:10204600-10217000 Weak transcription Placenta Placenta
16 chr11:10204800-10205600 Strong transcription NHDF-Ad bronchial
17 chr11:10205000-10205400 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
18 chr11:10205200-10205600 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
19 chr11:10205200-10206200 Enhancers Primary hematopoietic stem cells blood

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