Variant report

Variant rs2205867
Chromosome Location chr6:5717630-5717631
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:5707600-5724000 Weak transcription Thymus Thymus
2 chr6:5713400-5718200 Weak transcription Primary B cells from cord blood blood
3 chr6:5713800-5723400 Weak transcription Primary T cells from cord blood blood
4 chr6:5714600-5723600 Weak transcription HUES48 Cell Line embryonic stem cell
5 chr6:5714800-5722800 Weak transcription H9 Cell Line embryonic stem cell
6 chr6:5715800-5718000 ZNF genes & repeats Primary hematopoietic stem cells G-CSF-mobilized Male --
7 chr6:5716600-5717800 ZNF genes & repeats Fetal Intestine Small intestine
8 chr6:5717000-5717800 Enhancers Primary monocytes fromperipheralblood blood
9 chr6:5717200-5717800 ZNF genes & repeats Primary B cells from peripheral blood blood
10 chr6:5717400-5718400 Weak transcription Monocytes-CD14+_RO01746 blood
11 chr6:5717400-5729000 Weak transcription Fetal Stomach stomach
12 chr6:5717600-5718000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr6:5717600-5718400 Weak transcription Breast Myoepithelial Primary Cells Breast
14 chr6:5717600-5718800 Weak transcription Primary hematopoietic stem cells short term culture blood
15 chr6:5717600-5729000 Weak transcription Fetal Lung lung
16 chr6:5717600-5729600 Weak transcription Brain Substantia Nigra brain

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