Variant report

Variant rs562073921
Chromosome Location chr2:98141178-98141179
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:98139000-98142000 Weak transcription Fetal Brain Female brain
2 chr2:98139600-98142400 Weak transcription Primary B cells from cord blood blood
3 chr2:98140400-98141800 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
4 chr2:98140400-98142000 Weak transcription Placenta Amnion Placenta Amnion
5 chr2:98140400-98142200 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
6 chr2:98140600-98143800 Weak transcription Primary T cells from cord blood blood
7 chr2:98140800-98142400 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
8 chr2:98140800-98142400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
9 chr2:98140800-98152800 Weak transcription Rectal Mucosa Donor 29 rectum
10 chr2:98140800-98187600 Weak transcription Fetal Stomach stomach

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