Variant report

Variant rs2385891
Chromosome Location chr9:139596420-139596421
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:139590600-139600800 Enhancers Primary hematopoietic stem cells blood
2 chr9:139593800-139605600 Weak transcription Liver Liver
3 chr9:139594000-139598800 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
4 chr9:139596000-139597000 Bivalent Enhancer Rectal Mucosa Donor 29 rectum
5 chr9:139596000-139598000 Weak transcription Adipose Nuclei Adipose
6 chr9:139596000-139599000 Enhancers Primary B cells from cord blood blood
7 chr9:139596200-139598800 Enhancers Fetal Thymus thymus
8 chr9:139596200-139599800 Weak transcription K562 blood
9 chr9:139596200-139606200 Weak transcription Fetal Intestine Small intestine
10 chr9:139596400-139597400 Weak transcription GM12878-XiMat blood
11 chr9:139596400-139597600 Weak transcription Primary neutrophils fromperipheralblood blood
12 chr9:139596400-139597600 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
13 chr9:139596400-139597800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
14 chr9:139596400-139597800 Weak transcription Primary T cells from cord blood blood
15 chr9:139596400-139597800 Enhancers Primary hematopoietic stem cells short term culture blood
16 chr9:139596400-139598000 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
17 chr9:139596400-139600800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
18 chr9:139596400-139606200 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
19 chr9:139596400-139606200 Weak transcription Spleen Spleen

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