Variant report

Variant rs501894
Chromosome Location chr1:93467011-93467012
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:93463800-93467600 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
2 chr1:93465200-93468000 Enhancers Fetal Intestine Small intestine
3 chr1:93465600-93467200 Enhancers iPS-15b Cell Line embryonic stem cell
4 chr1:93465800-93467200 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
5 chr1:93465800-93467200 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
6 chr1:93466000-93467200 Enhancers Breast Myoepithelial Primary Cells Breast
7 chr1:93466000-93467200 Enhancers Fetal Lung lung
8 chr1:93466000-93467400 Enhancers Fetal Muscle Leg muscle
9 chr1:93466000-93468000 Enhancers Fetal Intestine Large intestine
10 chr1:93466200-93467200 Bivalent Enhancer Muscle Satellite Cultured Cells --
11 chr1:93466400-93467200 Enhancers HUES48 Cell Line embryonic stem cell
12 chr1:93466400-93467200 Enhancers HUES64 Cell Line embryonic stem cell
13 chr1:93466800-93467800 Enhancers Placenta Placenta
14 chr1:93467000-93470200 Weak transcription GM12878-XiMat blood
15 chr1:93467000-93474600 Weak transcription ES-I3 Cell Line embryonic stem cell

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