Variant report

Variant rs34755670
Chromosome Location chr9:139958645-139958646
allele A/C/G
Outlinks Ensembl   UCSC
Chromatin state (count:84 , 50 per page) page: 1 2
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:139949000-139963600 Weak transcription Placenta Amnion Placenta Amnion
2 chr9:139949200-139962400 Weak transcription K562 blood
3 chr9:139950600-139962400 Weak transcription Esophagus oesophagus
4 chr9:139950800-139958800 Weak transcription Ovary ovary
5 chr9:139950800-139959200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
6 chr9:139951800-139959800 Weak transcription Duodenum Mucosa Duodenum
7 chr9:139952200-139964000 Weak transcription Sigmoid Colon Sigmoid Colon
8 chr9:139952400-139963600 Weak transcription HSMM muscle
9 chr9:139953400-139959000 Weak transcription Hela-S3 cervix
10 chr9:139953400-139961600 Weak transcription Rectal Mucosa Donor 29 rectum
11 chr9:139953400-139962400 Weak transcription Rectal Mucosa Donor 31 rectum
12 chr9:139953600-139959000 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
13 chr9:139953600-139962600 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
14 chr9:139953800-139960600 Weak transcription HepG2 liver
15 chr9:139954200-139958800 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
16 chr9:139955600-139963000 Weak transcription Primary hematopoietic stem cells blood
17 chr9:139955600-139963200 Weak transcription NHLF lung
18 chr9:139956200-139962400 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
19 chr9:139956400-139959800 Weak transcription H9 Cell Line embryonic stem cell
20 chr9:139956400-139960000 Enhancers HMEC breast
21 chr9:139956600-139959600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
22 chr9:139956800-139958800 Enhancers Primary neutrophils fromperipheralblood blood
23 chr9:139956800-139959000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
24 chr9:139957400-139962400 Weak transcription Brain Hippocampus Middle brain
25 chr9:139957600-139959800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
26 chr9:139957600-139961200 Strong transcription Primary hematopoietic stem cells short term culture blood
27 chr9:139957600-139962000 Weak transcription Fetal Thymus thymus
28 chr9:139957800-139958800 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
29 chr9:139957800-139959800 Genic enhancers iPS DF 19.11 Cell Line embryonic stem cell
30 chr9:139957800-139960400 Strong transcription Thymus Thymus
31 chr9:139957800-139962400 Weak transcription NHEK skin
32 chr9:139958000-139958800 Enhancers Lung lung
33 chr9:139958000-139959000 Enhancers Cortex derived primary cultured neurospheres brain
34 chr9:139958000-139959000 Bivalent Enhancer Fetal Muscle Trunk muscle
35 chr9:139958000-139961200 Strong transcription Dnd41 blood
36 chr9:139958200-139958800 Enhancers A549 lung
37 chr9:139958200-139959000 Enhancers Brain Angular Gyrus brain
38 chr9:139958200-139959000 Enhancers Brain Inferior Temporal Lobe brain
39 chr9:139958200-139959000 Enhancers Brain Substantia Nigra brain
40 chr9:139958200-139959000 Enhancers Fetal Muscle Leg muscle
41 chr9:139958200-139959000 Enhancers Pancreas Pancrea
42 chr9:139958200-139959200 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
43 chr9:139958200-139959400 Flanking Active TSS Breast Myoepithelial Primary Cells Breast
44 chr9:139958200-139959400 Enhancers Placenta Placenta
45 chr9:139958400-139958800 Enhancers Primary monocytes fromperipheralblood blood
46 chr9:139958400-139958800 Enhancers Primary Natural Killer cells fromperipheralblood blood
47 chr9:139958400-139958800 Flanking Active TSS Foreskin Fibroblast Primary Cells skin02 Skin
48 chr9:139958400-139958800 Bivalent Enhancer Duodenum Smooth Muscle Duodenum
49 chr9:139958400-139958800 Enhancers Gastric stomach
50 chr9:139958400-139958800 Enhancers Right Ventricle heart

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