The 2.0 version of rSNPBase

Variant report

Variant rs11487433
Chromosome Location chr1:180709759-180709760
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:180704200-180710000 Weak transcription Breast Myoepithelial Primary Cells Breast
2 chr1:180704200-180711800 Weak transcription Primary T helper 17 cells PMA-I stimulated --
3 chr1:180704200-180713200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr1:180704400-180712600 Weak transcription K562 blood
5 chr1:180706400-180709800 Weak transcription Monocytes-CD14+_RO01746 blood
6 chr1:180706400-180711000 Weak transcription Primary T cells fromperipheralblood blood
7 chr1:180708000-180710800 Weak transcription Rectal Mucosa Donor 29 rectum
8 chr1:180708400-180722400 Weak transcription Aorta Aorta
9 chr1:180708600-180711400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
10 chr1:180708800-180710200 Strong transcription Left Ventricle heart
11 chr1:180709000-180710400 ZNF genes & repeats Primary hematopoietic stem cells G-CSF-mobilized Male --
12 chr1:180709200-180710400 ZNF genes & repeats Primary T cells from cord blood blood
13 chr1:180709400-180710000 ZNF genes & repeats Primary T cells effector/memory enriched fromperipheralblood blood
14 chr1:180709400-180710400 ZNF genes & repeats Primary hematopoietic stem cells blood
15 chr1:180709600-180710200 Strong transcription Primary B cells from cord blood blood
16 chr1:180709600-180710200 ZNF genes & repeats Primary T helper cells fromperipheralblood blood

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Last update: Aug 31, 2015