Variant report

Variant rs2277838
Chromosome Location chr22:21377650-21377651
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr22:21369600-21379400 Weak transcription Breast Myoepithelial Primary Cells Breast
2 chr22:21370200-21381400 Weak transcription Brain Dorsolateral Prefrontal Cortex brain
3 chr22:21370400-21382800 Weak transcription Brain Cingulate Gyrus brain
4 chr22:21370400-21383400 Weak transcription Brain Inferior Temporal Lobe brain
5 chr22:21370600-21382000 Weak transcription Psoas Muscle Psoas
6 chr22:21371000-21382200 Weak transcription Fetal Intestine Small intestine
7 chr22:21371600-21381000 Weak transcription HSMM muscle
8 chr22:21371600-21381400 Weak transcription HSMMtube muscle
9 chr22:21372000-21381200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
10 chr22:21372800-21379600 Weak transcription Skeletal Muscle Female skeletal muscle
11 chr22:21373000-21379600 Weak transcription Skeletal Muscle Male skeletal muscle
12 chr22:21376000-21379600 Weak transcription Right Atrium heart
13 chr22:21376000-21379800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
14 chr22:21376200-21379800 Weak transcription Placenta Placenta
15 chr22:21377200-21378000 Active TSS H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
16 chr22:21377400-21378000 Enhancers Fetal Thymus thymus
17 chr22:21377600-21377800 Enhancers Esophagus oesophagus
18 chr22:21377600-21378000 Strong transcription Fetal Muscle Leg muscle

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