The 2.0 version of rSNPBase

Variant report

Variant rs282006
Chromosome Location chr1:91863622-91863623
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:91853200-91866800 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
2 chr1:91853200-91869200 Weak transcription HUES6 Cell Line embryonic stem cell
3 chr1:91853200-91869200 Weak transcription Stomach Smooth Muscle stomach
4 chr1:91853200-91869400 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
5 chr1:91853200-91869600 Weak transcription Skeletal Muscle Female skeletal muscle
6 chr1:91857800-91866800 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
7 chr1:91861600-91869400 Weak transcription Primary hematopoietic stem cells blood
8 chr1:91862400-91864200 Enhancers Fetal Stomach stomach
9 chr1:91862400-91864200 Enhancers Rectal Smooth Muscle rectum
10 chr1:91862600-91864000 Enhancers Colon Smooth Muscle Colon
11 chr1:91863000-91864200 Enhancers Cortex derived primary cultured neurospheres brain
12 chr1:91863200-91864000 Enhancers Breast Myoepithelial Primary Cells Breast
13 chr1:91863200-91864400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
14 chr1:91863200-91864400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
15 chr1:91863600-91863800 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
16 chr1:91863600-91869400 Weak transcription ES-I3 Cell Line embryonic stem cell
17 chr1:91863600-91869600 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin

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Last update: Aug 31, 2015