Variant report

Variant rs11080644
Chromosome Location chr18:13327843-13327844
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr18:13317400-13331200 Weak transcription Primary T cells from cord blood blood
2 chr18:13320400-13338200 Weak transcription Small Intestine intestine
3 chr18:13321200-13329600 Weak transcription Fetal Heart heart
4 chr18:13321200-13336000 Weak transcription Left Ventricle heart
5 chr18:13321400-13328000 Weak transcription Breast Myoepithelial Primary Cells Breast
6 chr18:13323400-13332600 Weak transcription Brain Anterior Caudate brain
7 chr18:13323400-13335800 Weak transcription Aorta Aorta
8 chr18:13323600-13329600 Weak transcription Stomach Smooth Muscle stomach
9 chr18:13323600-13330800 Weak transcription Dnd41 blood
10 chr18:13325600-13328000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
11 chr18:13325600-13328000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
12 chr18:13326200-13328400 Enhancers Fetal Brain Female brain
13 chr18:13326200-13331200 Weak transcription Psoas Muscle Psoas
14 chr18:13327200-13328400 Enhancers Fetal Brain Male brain
15 chr18:13327800-13328000 ZNF genes & repeats Fetal Stomach stomach
16 chr18:13327800-13328200 ZNF genes & repeats Thymus Thymus
17 chr18:13327800-13328400 ZNF genes & repeats Primary hematopoietic stem cells blood
18 chr18:13327800-13328400 ZNF genes & repeats Primary hematopoietic stem cells G-CSF-mobilized Male --
19 chr18:13327800-13328600 ZNF genes & repeats Fetal Thymus thymus

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