Variant report

Variant rs6714558
Chromosome Location chr2:127890878-127890879
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:127870600-127898400 Weak transcription Right Atrium heart
2 chr2:127880200-127894000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
3 chr2:127886400-127891800 Weak transcription Brain Anterior Caudate brain
4 chr2:127886400-127892400 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
5 chr2:127886400-127893000 Weak transcription Brain Hippocampus Middle brain
6 chr2:127886400-127893000 Weak transcription Spleen Spleen
7 chr2:127886600-127891200 Weak transcription Monocytes-CD14+_RO01746 blood
8 chr2:127886600-127892200 Weak transcription Brain Inferior Temporal Lobe brain
9 chr2:127886600-127893000 Weak transcription Brain Angular Gyrus brain
10 chr2:127886600-127893000 Weak transcription Fetal Intestine Small intestine
11 chr2:127886600-127893600 Weak transcription Brain Substantia Nigra brain
12 chr2:127886800-127892200 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
13 chr2:127886800-127892200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
14 chr2:127890600-127891000 Enhancers Fetal Muscle Trunk muscle
15 chr2:127890600-127891200 Enhancers Fetal Muscle Leg muscle
16 chr2:127890800-127891200 Enhancers Placenta Placenta
17 chr2:127890800-127891600 Weak transcription Primary hematopoietic stem cells short term culture blood

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