Variant report

Variant rs143698805
Chromosome Location chr2:98143345-98143346
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:98140600-98143800 Weak transcription Primary T cells from cord blood blood
2 chr2:98140800-98152800 Weak transcription Rectal Mucosa Donor 29 rectum
3 chr2:98140800-98187600 Weak transcription Fetal Stomach stomach
4 chr2:98141200-98144800 Weak transcription Thymus Thymus
5 chr2:98141800-98144200 ZNF genes & repeats Primary hematopoietic stem cells G-CSF-mobilized Male --
6 chr2:98141800-98161000 Weak transcription Primary T helper cells fromperipheralblood blood
7 chr2:98141800-98162800 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
8 chr2:98142000-98168000 Weak transcription Primary T helper memory cells from peripheral blood 1 blood
9 chr2:98142400-98143600 Strong transcription Foreskin Melanocyte Primary Cells skin03 Skin
10 chr2:98142600-98143400 ZNF genes & repeats Ovary ovary
11 chr2:98142600-98144400 Weak transcription Brain Germinal Matrix brain
12 chr2:98142800-98153200 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
13 chr2:98142800-98155400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
14 chr2:98142800-98155800 Weak transcription Fetal Brain Female brain
15 chr2:98142800-98156000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
16 chr2:98142800-98162200 Weak transcription Primary B cells from cord blood blood
17 chr2:98142800-98165000 Weak transcription Placenta Amnion Placenta Amnion
18 chr2:98142800-98171400 Weak transcription Fetal Intestine Small intestine
19 chr2:98142800-98174800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
20 chr2:98142800-98177800 Weak transcription Cortex derived primary cultured neurospheres brain

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