Variant report

Variant rs4280369
Chromosome Location chr19:39525045-39525046
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:39523400-39529000 Weak transcription Esophagus oesophagus
2 chr19:39523400-39535400 Weak transcription Right Atrium heart
3 chr19:39523600-39525200 Enhancers Breast Myoepithelial Primary Cells Breast
4 chr19:39523800-39528400 Weak transcription HUES6 Cell Line embryonic stem cell
5 chr19:39523800-39528600 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
6 chr19:39523800-39528600 Weak transcription Brain Substantia Nigra brain
7 chr19:39523800-39528800 Weak transcription Brain Cingulate Gyrus brain
8 chr19:39523800-39528800 Weak transcription Brain Inferior Temporal Lobe brain
9 chr19:39523800-39528800 Weak transcription K562 blood
10 chr19:39524400-39527400 Weak transcription A549 lung
11 chr19:39524400-39528600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
12 chr19:39524600-39527400 Weak transcription Fetal Intestine Small intestine
13 chr19:39524600-39528600 Weak transcription Liver Liver
14 chr19:39524800-39528600 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
15 chr19:39525000-39526800 Weak transcription Fetal Intestine Large intestine
16 chr19:39525000-39528400 Weak transcription NHEK skin
17 chr19:39525000-39528600 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin

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