Variant report

Variant rs61765561
Chromosome Location chr1:57663695-57663696
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:57647000-57670600 Weak transcription Fetal Intestine Small intestine
2 chr1:57657400-57670200 Weak transcription Fetal Intestine Large intestine
3 chr1:57658000-57663800 Weak transcription Fetal Brain Male brain
4 chr1:57658400-57664200 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
5 chr1:57661400-57663800 Weak transcription ES-I3 Cell Line embryonic stem cell
6 chr1:57661600-57664200 Weak transcription iPS-20b Cell Line embryonic stem cell
7 chr1:57662000-57663800 Weak transcription HUES48 Cell Line embryonic stem cell
8 chr1:57662000-57664000 Weak transcription HUES6 Cell Line embryonic stem cell
9 chr1:57662200-57663800 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
10 chr1:57662200-57664600 Weak transcription Fetal Brain Female brain
11 chr1:57662800-57665200 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
12 chr1:57663200-57665400 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
13 chr1:57663600-57663800 Enhancers HUES64 Cell Line embryonic stem cell
14 chr1:57663600-57664000 Enhancers Cortex derived primary cultured neurospheres brain
15 chr1:57663600-57669800 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived

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