Variant report

Variant rs9605079
Chromosome Location chr22:20161295-20161296
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr22:20150000-20170000 Weak transcription Spleen Spleen
2 chr22:20157600-20171400 Strong transcription Right Atrium heart
3 chr22:20158200-20163200 Enhancers Liver Liver
4 chr22:20160000-20162400 Weak transcription Cortex derived primary cultured neurospheres brain
5 chr22:20160000-20164200 Weak transcription Gastric stomach
6 chr22:20160000-20165000 Weak transcription Brain Germinal Matrix brain
7 chr22:20160000-20165600 Weak transcription Fetal Brain Male brain
8 chr22:20160800-20162600 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
9 chr22:20160800-20162600 Enhancers Fetal Intestine Large intestine
10 chr22:20160800-20163000 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
11 chr22:20161000-20162400 Enhancers Fetal Intestine Small intestine
12 chr22:20161000-20162600 Genic enhancers iPS DF 19.11 Cell Line embryonic stem cell
13 chr22:20161000-20163400 Enhancers ES-UCSF4 Cell Line embryonic stem cell
14 chr22:20161200-20161600 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin01 Skin
15 chr22:20161200-20161600 Bivalent Enhancer HepG2 liver

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