Variant report

Variant rs535626267
Chromosome Location chr2:98141855-98141856
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 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 chr2:98140400-98142000 Weak transcription Placenta Amnion Placenta Amnion
4 chr2:98140400-98142200 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
5 chr2:98140600-98143800 Weak transcription Primary T cells from cord blood blood
6 chr2:98140800-98142400 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
7 chr2:98140800-98142400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
8 chr2:98140800-98152800 Weak transcription Rectal Mucosa Donor 29 rectum
9 chr2:98140800-98187600 Weak transcription Fetal Stomach stomach
10 chr2:98141200-98144800 Weak transcription Thymus Thymus
11 chr2:98141800-98144200 ZNF genes & repeats Primary hematopoietic stem cells G-CSF-mobilized Male --
12 chr2:98141800-98161000 Weak transcription Primary T helper cells fromperipheralblood blood
13 chr2:98141800-98162800 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --

Quick Search:


  
Input of quick search could be:

what's new

Quick links