Variant report

Variant rs11620583
Chromosome Location chr13:52568093-52568094
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:52553400-52569400 Weak transcription Pancreas Pancrea
2 chr13:52555600-52568800 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
3 chr13:52555800-52569200 Weak transcription Left Ventricle heart
4 chr13:52555800-52570200 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
5 chr13:52562200-52569400 Weak transcription Fetal Intestine Large intestine
6 chr13:52563400-52569200 Weak transcription Duodenum Mucosa Duodenum
7 chr13:52563600-52569200 Weak transcription Stomach Mucosa stomach
8 chr13:52566000-52569200 Weak transcription Fetal Intestine Small intestine
9 chr13:52567200-52568800 Active TSS K562 blood
10 chr13:52567400-52568200 Enhancers Fetal Lung lung
11 chr13:52567400-52568400 Flanking Active TSS Primary hematopoietic stem cells G-CSF-mobilized Male --
12 chr13:52567400-52568400 Enhancers Liver Liver
13 chr13:52567400-52571200 Genic enhancers HepG2 liver
14 chr13:52567800-52568400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
15 chr13:52568000-52569400 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
16 chr13:52568000-52569600 Enhancers Primary hematopoietic stem cells short term culture blood

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