The 2.0 version of rSNPBase

Variant report

Variant rs12119202
Chromosome Location chr1:45925931-45925932
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:45889800-45940600 Weak transcription Primary neutrophils fromperipheralblood blood
2 chr1:45911000-45930400 Weak transcription Psoas Muscle Psoas
3 chr1:45913000-45931000 Weak transcription Sigmoid Colon Sigmoid Colon
4 chr1:45913000-45933000 Weak transcription Ovary ovary
5 chr1:45915400-45940600 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
6 chr1:45915600-45929600 Weak transcription Left Ventricle heart
7 chr1:45917000-45930000 Weak transcription Aorta Aorta
8 chr1:45919000-45941000 Weak transcription Fetal Intestine Small intestine
9 chr1:45920600-45932600 Weak transcription GM12878-XiMat blood
10 chr1:45921200-45933800 Weak transcription Brain Hippocampus Middle brain
11 chr1:45921200-45934200 Weak transcription Brain Substantia Nigra brain
12 chr1:45921800-45933000 Weak transcription Primary B cells from peripheral blood blood
13 chr1:45923400-45928000 Weak transcription Rectal Mucosa Donor 29 rectum
14 chr1:45923400-45940600 Weak transcription Primary B cells from cord blood blood
15 chr1:45923600-45951600 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
16 chr1:45925200-45926400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
17 chr1:45925400-45926000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin

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Last update: Aug 31, 2015