Variant report

Variant rs61767400
Chromosome Location chr1:57771199-57771200
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:57769400-57771200 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
2 chr1:57769800-57771600 Weak transcription Fetal Heart heart
3 chr1:57770000-57775400 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
4 chr1:57770200-57772000 Weak transcription Primary T helper cells PMA-I stimulated --
5 chr1:57770400-57772600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
6 chr1:57770400-57772600 Enhancers Primary T helper 17 cells PMA-I stimulated --
7 chr1:57770400-57772800 Weak transcription ES-I3 Cell Line embryonic stem cell
8 chr1:57770600-57771200 Genic enhancers Fetal Intestine Small intestine
9 chr1:57770600-57772600 Genic enhancers Fetal Intestine Large intestine
10 chr1:57770800-57776000 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
11 chr1:57771000-57771200 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
12 chr1:57771000-57771600 Weak transcription Primary T helper memory cells from peripheral blood 2 blood
13 chr1:57771000-57772000 Weak transcription Primary T helper cells fromperipheralblood blood
14 chr1:57771000-57773400 Weak transcription HepG2 liver
15 chr1:57771000-57773800 Enhancers Primary T regulatory cells fromperipheralblood blood

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