Variant report

Variant rs333434
Chromosome Location chr1:174710148-174710149
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:174705800-174712200 Weak transcription Left Ventricle heart
2 chr1:174706000-174730400 Weak transcription Aorta Aorta
3 chr1:174706200-174734000 Weak transcription Primary B cells from peripheral blood blood
4 chr1:174707200-174715000 Weak transcription Fetal Heart heart
5 chr1:174707600-174712200 Weak transcription Liver Liver
6 chr1:174708000-174722000 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
7 chr1:174708600-174710600 Enhancers Fetal Intestine Large intestine
8 chr1:174709200-174711400 Enhancers Monocytes-CD14+_RO01746 blood
9 chr1:174709200-174713200 Enhancers Primary neutrophils fromperipheralblood blood
10 chr1:174709400-174710200 Enhancers GM12878-XiMat blood
11 chr1:174709400-174711800 Enhancers Primary B cells from cord blood blood
12 chr1:174709400-174712600 Enhancers Primary monocytes fromperipheralblood blood
13 chr1:174709600-174713400 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
14 chr1:174709800-174710600 Enhancers Fetal Intestine Small intestine
15 chr1:174709800-174711800 Weak transcription Muscle Satellite Cultured Cells --
16 chr1:174709800-174712000 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived

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