Variant report

Variant rs6830286
Chromosome Location chr4:101009287-101009288
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:101006600-101009800 Enhancers Placenta Placenta
2 chr4:101007800-101028000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
3 chr4:101008200-101009800 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
4 chr4:101008600-101009600 Flanking Active TSS Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
5 chr4:101008600-101009600 Enhancers Adipose Nuclei Adipose
6 chr4:101008600-101014000 Weak transcription iPS-18 Cell Line embryonic stem cell
7 chr4:101008600-101014200 Weak transcription HUES6 Cell Line embryonic stem cell
8 chr4:101008600-101017800 Weak transcription Placenta Amnion Placenta Amnion
9 chr4:101008800-101014200 Weak transcription HUES64 Cell Line embryonic stem cell
10 chr4:101008800-101014200 Weak transcription iPS-15b Cell Line embryonic stem cell
11 chr4:101008800-101014200 Weak transcription iPS-20b Cell Line embryonic stem cell
12 chr4:101009000-101010200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
13 chr4:101009000-101014400 Weak transcription NHEK skin
14 chr4:101009200-101009800 Enhancers Fetal Lung lung
15 chr4:101009200-101013600 Weak transcription ES-I3 Cell Line embryonic stem cell
16 chr4:101009200-101013800 Weak transcription Fetal Stomach stomach
17 chr4:101009200-101014400 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
18 chr4:101009200-101017600 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin

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