Variant report

Variant rs2026014
Chromosome Location chr1:179545999-179546000
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:179543200-179546400 Bivalent/Poised TSS Fetal Kidney kidney
2 chr1:179545200-179546000 Bivalent Enhancer Primary B cells from peripheral blood blood
3 chr1:179545400-179546000 Bivalent Enhancer iPS DF 19.11 Cell Line embryonic stem cell
4 chr1:179545600-179546000 Bivalent Enhancer HUES6 Cell Line embryonic stem cell
5 chr1:179545600-179546000 Flanking Bivalent TSS/Enh iPS-18 Cell Line embryonic stem cell
6 chr1:179545600-179546000 Enhancers ES-UCSF4 Cell Line embryonic stem cell
7 chr1:179545600-179546000 Bivalent/Poised TSS Primary hematopoietic stem cells G-CSF-mobilized Female --
8 chr1:179545600-179546000 Bivalent Enhancer Small Intestine intestine
9 chr1:179545800-179546000 Bivalent Enhancer HUES48 Cell Line embryonic stem cell
10 chr1:179545800-179546000 Flanking Bivalent TSS/Enh HUES64 Cell Line embryonic stem cell
11 chr1:179545800-179546000 Flanking Bivalent TSS/Enh iPS-15b Cell Line embryonic stem cell
12 chr1:179545800-179546000 Bivalent Enhancer Primary T regulatory cells fromperipheralblood blood
13 chr1:179545800-179546000 Flanking Bivalent TSS/Enh Primary hematopoietic stem cells G-CSF-mobilized Male --
14 chr1:179545800-179546000 Flanking Bivalent TSS/Enh Duodenum Mucosa Duodenum
15 chr1:179545800-179546000 Bivalent Enhancer Skeletal Muscle Female skeletal muscle
16 chr1:179545800-179546200 Bivalent Enhancer iPS-20b Cell Line embryonic stem cell

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