Variant report

Variant rs398074822
Chromosome Location chr1:246645763-246645764
allele -/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:246621600-246646400 Weak transcription Primary B cells from cord blood blood
2 chr1:246623200-246646600 Weak transcription Primary hematopoietic stem cells short term culture blood
3 chr1:246623600-246663200 Weak transcription Primary T cells from cord blood blood
4 chr1:246632400-246647000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
5 chr1:246640400-246646200 Weak transcription Primary T helper cells PMA-I stimulated --
6 chr1:246640800-246646200 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
7 chr1:246641000-246645800 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
8 chr1:246641000-246646000 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
9 chr1:246641200-246646200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
10 chr1:246641400-246646000 Weak transcription Primary T regulatory cells fromperipheralblood blood
11 chr1:246641400-246646800 Weak transcription Primary T killer memory cells from peripheral blood blood
12 chr1:246644200-246646200 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
13 chr1:246644800-246648400 Weak transcription Primary T cells effector/memory enriched fromperipheralblood blood
14 chr1:246645400-246646200 Enhancers Small Intestine intestine
15 chr1:246645600-246646000 Enhancers GM12878-XiMat blood
16 chr1:246645600-246646400 Enhancers Esophagus oesophagus
17 chr1:246645600-246647200 Enhancers Primary B cells from peripheral blood blood

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