Variant report

Variant rs184270822
Chromosome Location chr5:177807743-177807744
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:177798800-177816400 Weak transcription Right Atrium heart
2 chr5:177802600-177807800 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
3 chr5:177804000-177808600 Weak transcription Fetal Intestine Small intestine
4 chr5:177804600-177809600 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
5 chr5:177804800-177812800 Weak transcription Spleen Spleen
6 chr5:177805000-177809200 Weak transcription Fetal Thymus thymus
7 chr5:177805000-177809600 Weak transcription Thymus Thymus
8 chr5:177805000-177814800 Weak transcription Gastric stomach
9 chr5:177805800-177808000 Enhancers Fetal Stomach stomach
10 chr5:177806400-177809600 Weak transcription Cortex derived primary cultured neurospheres brain
11 chr5:177806600-177809400 Weak transcription Fetal Lung lung
12 chr5:177806600-177809600 Weak transcription Fetal Intestine Large intestine
13 chr5:177807000-177810200 Enhancers HSMMtube muscle
14 chr5:177807200-177808800 Enhancers Fetal Muscle Trunk muscle
15 chr5:177807200-177810400 Enhancers Fetal Muscle Leg muscle
16 chr5:177807400-177810800 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
17 chr5:177807600-177808200 Enhancers iPS DF 19.11 Cell Line embryonic stem cell

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