Variant report

Variant rs745876
Chromosome Location chr9:695143-695144
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:100 , 50 per page) page: 1 2
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:653400-698000 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
2 chr9:670800-706800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
3 chr9:678000-695200 Weak transcription Colonic Mucosa Colon
4 chr9:682800-696800 Enhancers Placenta Amnion Placenta Amnion
5 chr9:688400-698000 Weak transcription Gastric stomach
6 chr9:688800-695200 Weak transcription Primary B cells from peripheral blood blood
7 chr9:690400-697000 Enhancers Stomach Mucosa stomach
8 chr9:690800-700600 Weak transcription Small Intestine intestine
9 chr9:691000-698400 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
10 chr9:691200-706600 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
11 chr9:692000-695400 Enhancers Primary hematopoietic stem cells short term culture blood
12 chr9:692000-697400 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
13 chr9:692000-698800 Enhancers Breast Myoepithelial Primary Cells Breast
14 chr9:692200-697600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
15 chr9:692600-695600 Flanking Active TSS Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
16 chr9:692600-696600 Enhancers Fetal Intestine Large intestine
17 chr9:692800-695200 Enhancers Dnd41 blood
18 chr9:692800-695600 Flanking Active TSS NHEK skin
19 chr9:692800-695800 Enhancers Fetal Intestine Small intestine
20 chr9:692800-695800 Flanking Active TSS HUVEC blood vessel
21 chr9:692800-696000 Enhancers Fetal Thymus thymus
22 chr9:692800-696600 Enhancers Fetal Adrenal Gland Adrenal Gland
23 chr9:693000-695400 Enhancers HUES64 Cell Line embryonic stem cell
24 chr9:693000-695400 Flanking Active TSS NH-A brain
25 chr9:693000-695600 Flanking Active TSS Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
26 chr9:693000-695600 Flanking Active TSS A549 lung
27 chr9:693200-695200 Active TSS Foreskin Melanocyte Primary Cells skin01 Skin
28 chr9:693200-695400 Flanking Active TSS Osteobl bone
29 chr9:693200-695600 Flanking Active TSS Muscle Satellite Cultured Cells --
30 chr9:693200-695600 Flanking Active TSS HSMM muscle
31 chr9:693200-697200 Active TSS Aorta Aorta
32 chr9:693400-695200 Flanking Active TSS Liver Liver
33 chr9:693600-695600 Enhancers Pancreas Pancrea
34 chr9:693600-696000 Enhancers Esophagus oesophagus
35 chr9:693600-697400 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
36 chr9:693800-695200 Enhancers Pancreatic Islets Pancreatic Islet
37 chr9:693800-695400 Flanking Active TSS NHLF lung
38 chr9:693800-696400 Weak transcription ES-I3 Cell Line embryonic stem cell
39 chr9:693800-696400 Weak transcription HUES6 Cell Line embryonic stem cell
40 chr9:693800-700400 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
41 chr9:693800-700400 Weak transcription iPS-15b Cell Line embryonic stem cell
42 chr9:693800-700600 Weak transcription H9 Cell Line embryonic stem cell
43 chr9:694000-695200 Flanking Active TSS Rectal Smooth Muscle rectum
44 chr9:694000-695600 Flanking Active TSS Ganglion Eminence derived primary cultured neurospheres brain
45 chr9:694000-696000 Flanking Active TSS Adipose Nuclei Adipose
46 chr9:694000-697000 Enhancers Fetal Stomach stomach
47 chr9:694000-697000 Flanking Active TSS Stomach Smooth Muscle stomach
48 chr9:694000-698000 Weak transcription HUES48 Cell Line embryonic stem cell
49 chr9:694000-698200 Weak transcription H1 Cell Line embryonic stem cell
50 chr9:694200-695200 Flanking Active TSS Fetal Muscle Leg muscle

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