Variant report

Variant rs17179136
Chromosome Location chr6:29802978-29802979
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:29796800-29803000 Weak transcription Pancreas Pancrea
2 chr6:29797000-29803000 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
3 chr6:29802600-29803000 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
4 chr6:29802600-29803200 Bivalent/Poised TSS iPS-15b Cell Line embryonic stem cell
5 chr6:29802600-29803200 Bivalent Enhancer Primary T cells fromperipheralblood blood
6 chr6:29802600-29803200 Enhancers Liver Liver
7 chr6:29802800-29803000 Bivalent Enhancer Primary T helper memory cells from peripheral blood 2 blood
8 chr6:29802800-29803000 Bivalent Enhancer Primary T helper naive cells fromperipheralblood blood
9 chr6:29802800-29803000 Bivalent Enhancer Primary T helper memory cells from peripheral blood 1 blood
10 chr6:29802800-29803000 Bivalent Enhancer Primary T helper 17 cells PMA-I stimulated --
11 chr6:29802800-29803000 Bivalent Enhancer Primary T helper cells fromperipheralblood blood
12 chr6:29802800-29803000 Bivalent Enhancer Primary mononuclear cells fromperipheralblood Blood
13 chr6:29802800-29803200 Bivalent Enhancer Primary hematopoietic stem cells G-CSF-mobilized Female --

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