Variant report

Variant rs10400832
Chromosome Location chr15:31361821-31361822
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:22 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr15:31353200-31363400 Weak transcription Right Atrium heart
2 chr15:31353400-31365200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
3 chr15:31354400-31363200 Weak transcription Left Ventricle heart
4 chr15:31355600-31362000 Weak transcription Spleen Spleen
5 chr15:31355600-31367800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
6 chr15:31359600-31363400 Enhancers Ovary ovary
7 chr15:31360000-31363600 Strong transcription Foreskin Melanocyte Primary Cells skin03 Skin
8 chr15:31360000-31363600 Enhancers Adipose Nuclei Adipose
9 chr15:31360200-31362600 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
10 chr15:31360400-31362800 Enhancers Liver Liver
11 chr15:31361000-31362400 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
12 chr15:31361200-31362400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
13 chr15:31361200-31362400 Enhancers Osteobl bone
14 chr15:31361400-31362000 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
15 chr15:31361400-31362000 Genic enhancers Foreskin Melanocyte Primary Cells skin01 Skin
16 chr15:31361400-31362000 Flanking Active TSS HepG2 liver
17 chr15:31361400-31362200 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
18 chr15:31361400-31362400 Enhancers Colon Smooth Muscle Colon
19 chr15:31361400-31362400 Enhancers HSMMtube muscle
20 chr15:31361600-31362000 Enhancers Small Intestine intestine
21 chr15:31361600-31362200 Weak transcription Fetal Kidney kidney
22 chr15:31361800-31362200 Enhancers Brain Substantia Nigra brain

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