Variant report

Variant rs7711896
Chromosome Location chr5:145581548-145581549
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:145563000-145582200 Weak transcription Right Atrium heart
2 chr5:145571000-145582400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
3 chr5:145577200-145582000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
4 chr5:145577800-145582400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
5 chr5:145578200-145582000 Weak transcription Fetal Lung lung
6 chr5:145579800-145582000 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
7 chr5:145580600-145582000 Weak transcription H1 Cell Line embryonic stem cell
8 chr5:145580600-145582000 Weak transcription HUES64 Cell Line embryonic stem cell
9 chr5:145580600-145582000 Weak transcription iPS-18 Cell Line embryonic stem cell
10 chr5:145580800-145581600 Weak transcription A549 lung
11 chr5:145580800-145582000 Weak transcription ES-I3 Cell Line embryonic stem cell
12 chr5:145580800-145582000 Weak transcription HUES48 Cell Line embryonic stem cell
13 chr5:145580800-145582000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
14 chr5:145580800-145582200 Weak transcription Fetal Stomach stomach
15 chr5:145581000-145582000 Weak transcription Primary T helper cells fromperipheralblood blood
16 chr5:145581400-145581800 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
17 chr5:145581400-145582000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
18 chr5:145581400-145582000 Enhancers HepG2 liver
19 chr5:145581400-145582000 Enhancers K562 blood

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