Variant report

Variant rs12073468
Chromosome Location chr1:225566546-225566547
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:225563400-225566600 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
2 chr1:225564400-225577600 Weak transcription Fetal Intestine Small intestine
3 chr1:225565800-225566800 Enhancers ES-I3 Cell Line embryonic stem cell
4 chr1:225565800-225567200 Enhancers NHEK skin
5 chr1:225565800-225568000 Enhancers HUES48 Cell Line embryonic stem cell
6 chr1:225565800-225568200 Enhancers HUES64 Cell Line embryonic stem cell
7 chr1:225565800-225568200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
8 chr1:225566000-225567200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
9 chr1:225566000-225567200 Enhancers HMEC breast
10 chr1:225566000-225567400 Enhancers HUES6 Cell Line embryonic stem cell
11 chr1:225566000-225567800 Enhancers iPS-20b Cell Line embryonic stem cell
12 chr1:225566000-225568200 Enhancers iPS-15b Cell Line embryonic stem cell
13 chr1:225566200-225566600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
14 chr1:225566200-225567000 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
15 chr1:225566200-225567000 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
16 chr1:225566400-225567000 Enhancers Placenta Placenta
17 chr1:225566400-225567600 Weak transcription ES-WA7 Cell Line embryonic stem cell

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