Variant report

Variant rs16825020
Chromosome Location chr1:186147404-186147405
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:22 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:186114600-186160800 Weak transcription Fetal Kidney kidney
2 chr1:186133600-186160800 Weak transcription HUES6 Cell Line embryonic stem cell
3 chr1:186133800-186147800 Weak transcription Left Ventricle heart
4 chr1:186134600-186152200 Weak transcription NH-A brain
5 chr1:186135000-186147800 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
6 chr1:186136200-186152400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
7 chr1:186136200-186153200 Weak transcription Fetal Lung lung
8 chr1:186136200-186157600 Weak transcription Duodenum Smooth Muscle Duodenum
9 chr1:186136800-186157000 Weak transcription Aorta Aorta
10 chr1:186137000-186152800 Weak transcription Liver Liver
11 chr1:186137200-186152000 Weak transcription Adipose Nuclei Adipose
12 chr1:186139200-186147600 Weak transcription NHDF-Ad bronchial
13 chr1:186140200-186148000 Weak transcription Right Atrium heart
14 chr1:186145000-186147800 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
15 chr1:186145000-186158400 Weak transcription Breast Myoepithelial Primary Cells Breast
16 chr1:186145400-186151200 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
17 chr1:186147000-186148400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
18 chr1:186147000-186148600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
19 chr1:186147000-186148800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
20 chr1:186147000-186148800 Enhancers HMEC breast
21 chr1:186147200-186148600 Enhancers NHEK skin
22 chr1:186147400-186148000 Strong transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived

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