Variant report

Variant rs7522479
Chromosome Location chr1:246964473-246964474
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:246958400-246966800 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
2 chr1:246960000-246964800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
3 chr1:246962400-246965800 Weak transcription Placenta Placenta
4 chr1:246962800-246965800 Weak transcription Right Ventricle heart
5 chr1:246963400-246964600 Weak transcription Fetal Muscle Leg muscle
6 chr1:246963800-246964800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr1:246963800-246964800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
8 chr1:246963800-246964800 Bivalent Enhancer NHEK skin
9 chr1:246964000-246964800 Enhancers HSMM muscle
10 chr1:246964200-246965200 Flanking Active TSS HepG2 liver
11 chr1:246964200-246966000 Enhancers Duodenum Mucosa Duodenum
12 chr1:246964200-246966000 Enhancers Fetal Intestine Large intestine
13 chr1:246964400-246964600 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
14 chr1:246964400-246965000 Enhancers Fetal Heart heart
15 chr1:246964400-246965400 Weak transcription Fetal Intestine Small intestine
16 chr1:246964400-246965400 Enhancers Fetal Muscle Trunk muscle
17 chr1:246964400-246965800 Enhancers HSMMtube muscle
18 chr1:246964400-246973000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell

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