The 2.0 version of rSNPBase

Variant report

Variant rs61767398
Chromosome Location chr1:57768178-57768179
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:57747600-57769400 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
2 chr1:57751600-57770600 Weak transcription Fetal Intestine Large intestine
3 chr1:57763600-57769000 Weak transcription Fetal Brain Male brain
4 chr1:57766400-57769400 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
5 chr1:57767200-57769400 Weak transcription iPS-15b Cell Line embryonic stem cell
6 chr1:57767200-57769800 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
7 chr1:57767200-57771000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
8 chr1:57767400-57769400 Enhancers Primary T helper 17 cells PMA-I stimulated --
9 chr1:57767600-57769200 Weak transcription H9 Cell Line embryonic stem cell
10 chr1:57767800-57770600 Weak transcription Fetal Intestine Small intestine
11 chr1:57768000-57768200 Enhancers Fetal Brain Female brain
12 chr1:57768000-57769000 Weak transcription HUES64 Cell Line embryonic stem cell

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Last update: Aug 31, 2015