Variant report

Variant rs56998902
Chromosome Location chr11:16852690-16852691
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:67 , 50 per page) page: 1 2
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:16813200-16871400 Weak transcription Rectal Smooth Muscle rectum
2 chr11:16823000-16871400 Weak transcription H9 Cell Line embryonic stem cell
3 chr11:16836000-16861600 Weak transcription Duodenum Smooth Muscle Duodenum
4 chr11:16839200-16878800 Weak transcription Thymus Thymus
5 chr11:16842400-16862200 Weak transcription Fetal Kidney kidney
6 chr11:16842600-16853600 Weak transcription HUES48 Cell Line embryonic stem cell
7 chr11:16842600-16854200 Weak transcription HUES6 Cell Line embryonic stem cell
8 chr11:16842600-16855000 Weak transcription iPS-15b Cell Line embryonic stem cell
9 chr11:16842600-16873400 Weak transcription Hela-S3 cervix
10 chr11:16842800-16862200 Weak transcription iPS-20b Cell Line embryonic stem cell
11 chr11:16843000-16874600 Weak transcription ES-I3 Cell Line embryonic stem cell
12 chr11:16844000-16862000 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
13 chr11:16844400-16861200 Weak transcription HMEC breast
14 chr11:16845800-16855200 Strong transcription HepG2 liver
15 chr11:16846200-16857800 Strong transcription Breast Myoepithelial Primary Cells Breast
16 chr11:16846400-16852800 Strong transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
17 chr11:16846600-16874000 Weak transcription Pancreatic Islets Pancreatic Islet
18 chr11:16847000-16864000 Weak transcription Brain Inferior Temporal Lobe brain
19 chr11:16847000-16871200 Weak transcription Brain Substantia Nigra brain
20 chr11:16847200-16871400 Weak transcription Brain Hippocampus Middle brain
21 chr11:16847600-16852800 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
22 chr11:16847600-16857000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
23 chr11:16847800-16853000 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
24 chr11:16847800-16865000 Weak transcription Fetal Muscle Leg muscle
25 chr11:16847800-16871600 Weak transcription Fetal Muscle Trunk muscle
26 chr11:16848000-16853000 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
27 chr11:16848000-16853800 Weak transcription Right Atrium heart
28 chr11:16848000-16854200 Weak transcription Brain Anterior Caudate brain
29 chr11:16848000-16862400 Weak transcription Adipose Nuclei Adipose
30 chr11:16848000-16863000 Weak transcription Lung lung
31 chr11:16848200-16853000 Weak transcription A549 lung
32 chr11:16848200-16853400 Weak transcription iPS-18 Cell Line embryonic stem cell
33 chr11:16848200-16853800 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
34 chr11:16848200-16854200 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
35 chr11:16848200-16854200 Weak transcription Left Ventricle heart
36 chr11:16848200-16854600 Weak transcription Fetal Stomach stomach
37 chr11:16848200-16854600 Weak transcription Spleen Spleen
38 chr11:16848200-16855000 Weak transcription H1 Cell Line embryonic stem cell
39 chr11:16848200-16857200 Weak transcription Placenta Amnion Placenta Amnion
40 chr11:16848200-16857600 Strong transcription Fetal Adrenal Gland Adrenal Gland
41 chr11:16848200-16861200 Weak transcription Stomach Smooth Muscle stomach
42 chr11:16848200-16861400 Weak transcription Ovary ovary
43 chr11:16848200-16862400 Weak transcription Esophagus oesophagus
44 chr11:16848200-16863000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
45 chr11:16848200-16871400 Weak transcription Aorta Aorta
46 chr11:16848200-16875200 Weak transcription Right Ventricle heart
47 chr11:16848400-16866600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
48 chr11:16848400-16878600 Weak transcription Small Intestine intestine
49 chr11:16848600-16868400 Weak transcription HSMMtube muscle
50 chr11:16849200-16861600 Weak transcription Sigmoid Colon Sigmoid Colon

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