Variant report

Variant rs3861026
Chromosome Location chr9:139662600-139662601
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:24 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:139655600-139664400 Weak transcription Pancreas Pancrea
2 chr9:139657600-139664200 Weak transcription Right Ventricle heart
3 chr9:139657800-139667800 Weak transcription Right Atrium heart
4 chr9:139658400-139664200 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
5 chr9:139658400-139664200 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
6 chr9:139658800-139662800 Enhancers Rectal Mucosa Donor 31 rectum
7 chr9:139659200-139667800 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
8 chr9:139659400-139663600 Enhancers Primary B cells from peripheral blood blood
9 chr9:139659800-139662600 Weak transcription Spleen Spleen
10 chr9:139660200-139663000 Enhancers Primary B cells from cord blood blood
11 chr9:139660600-139662800 Enhancers Primary Natural Killer cells fromperipheralblood blood
12 chr9:139660800-139663000 Enhancers GM12878-XiMat blood
13 chr9:139661400-139664200 Weak transcription Brain Inferior Temporal Lobe brain
14 chr9:139661600-139662800 Enhancers K562 blood
15 chr9:139662200-139662600 Bivalent Enhancer Duodenum Mucosa Duodenum
16 chr9:139662200-139662800 Enhancers Fetal Thymus thymus
17 chr9:139662400-139662600 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
18 chr9:139662400-139662600 Bivalent Enhancer Rectal Mucosa Donor 29 rectum
19 chr9:139662400-139662800 Flanking Active TSS HepG2 liver
20 chr9:139662600-139662800 Bivalent Enhancer H1 Derived Mesenchymal Stem Cells ES cell derived
21 chr9:139662600-139662800 Genic enhancers iPS DF 19.11 Cell Line embryonic stem cell
22 chr9:139662600-139662800 Flanking Active TSS Primary mononuclear cells fromperipheralblood Blood
23 chr9:139662600-139662800 Bivalent Enhancer Placenta Placenta
24 chr9:139662600-139662800 Enhancers Spleen Spleen

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