Variant report

Variant rs528660737
Chromosome Location chr2:98142124-98142125
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:98139600-98142400 Weak transcription Primary B cells from cord blood blood
2 chr2:98140400-98142200 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
3 chr2:98140600-98143800 Weak transcription Primary T cells from cord blood blood
4 chr2:98140800-98142400 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
5 chr2:98140800-98142400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
6 chr2:98140800-98152800 Weak transcription Rectal Mucosa Donor 29 rectum
7 chr2:98140800-98187600 Weak transcription Fetal Stomach stomach
8 chr2:98141200-98144800 Weak transcription Thymus Thymus
9 chr2:98141800-98144200 ZNF genes & repeats Primary hematopoietic stem cells G-CSF-mobilized Male --
10 chr2:98141800-98161000 Weak transcription Primary T helper cells fromperipheralblood blood
11 chr2:98141800-98162800 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
12 chr2:98142000-98142800 ZNF genes & repeats Foreskin Keratinocyte Primary Cells skin02 Skin
13 chr2:98142000-98142800 ZNF genes & repeats Fetal Brain Female brain
14 chr2:98142000-98142800 Strong transcription Placenta Amnion Placenta Amnion
15 chr2:98142000-98168000 Weak transcription Primary T helper memory cells from peripheral blood 1 blood

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