Variant report

Variant rs553417342
Chromosome Location chr14:105294754-105294755
allele -/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:105294200-105294800 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
2 chr14:105294200-105297200 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
3 chr14:105294200-105298600 Weak transcription Right Atrium heart
4 chr14:105294200-105300800 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
5 chr14:105294400-105294800 Enhancers Rectal Mucosa Donor 31 rectum
6 chr14:105294400-105295400 Weak transcription K562 blood
7 chr14:105294400-105297000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
8 chr14:105294400-105297200 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
9 chr14:105294400-105297400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
10 chr14:105294600-105294800 Enhancers Duodenum Mucosa Duodenum
11 chr14:105294600-105297000 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
12 chr14:105294600-105297000 Weak transcription Fetal Intestine Small intestine
13 chr14:105294600-105301400 Weak transcription Adipose Nuclei Adipose

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