Variant report

Variant rs17018663
Chromosome Location chr2:36610325-36610326
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:85 , 50 per page) page: 1 2
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:36586200-36626600 Weak transcription Primary B cells from cord blood blood
2 chr2:36600400-36612000 Genic enhancers Osteobl bone
3 chr2:36603800-36612600 Weak transcription Fetal Brain Female brain
4 chr2:36604000-36614400 Genic enhancers HUVEC blood vessel
5 chr2:36604000-36617000 Weak transcription Primary hematopoietic stem cells blood
6 chr2:36604400-36611200 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
7 chr2:36604400-36614000 Weak transcription HSMMtube muscle
8 chr2:36604400-36615000 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
9 chr2:36604400-36615400 Weak transcription Cortex derived primary cultured neurospheres brain
10 chr2:36604400-36615600 Weak transcription Fetal Muscle Leg muscle
11 chr2:36604400-36616400 Weak transcription Gastric stomach
12 chr2:36604400-36620600 Weak transcription Fetal Brain Male brain
13 chr2:36604400-36640400 Weak transcription Brain Inferior Temporal Lobe brain
14 chr2:36604400-36640600 Weak transcription Brain Cingulate Gyrus brain
15 chr2:36604600-36614800 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
16 chr2:36604600-36617600 Genic enhancers Breast Myoepithelial Primary Cells Breast
17 chr2:36604600-36620800 Weak transcription Brain Hippocampus Middle brain
18 chr2:36604800-36614400 Weak transcription Rectal Smooth Muscle rectum
19 chr2:36607000-36611600 Genic enhancers NHLF lung
20 chr2:36607600-36620800 Weak transcription Pancreas Pancrea
21 chr2:36607800-36615800 Weak transcription Rectal Mucosa Donor 29 rectum
22 chr2:36608000-36610800 Weak transcription iPS-20b Cell Line embryonic stem cell
23 chr2:36608000-36614000 Weak transcription Hela-S3 cervix
24 chr2:36608000-36614600 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
25 chr2:36608200-36612200 Weak transcription Colon Smooth Muscle Colon
26 chr2:36608400-36611200 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
27 chr2:36608600-36610600 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
28 chr2:36608600-36611200 Weak transcription Esophagus oesophagus
29 chr2:36608600-36611600 Genic enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
30 chr2:36608600-36612600 Weak transcription Right Atrium heart
31 chr2:36608600-36612600 Weak transcription Small Intestine intestine
32 chr2:36608600-36614000 Weak transcription Placenta Amnion Placenta Amnion
33 chr2:36608600-36614000 Weak transcription Sigmoid Colon Sigmoid Colon
34 chr2:36608600-36616200 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
35 chr2:36608600-36616200 Weak transcription Fetal Stomach stomach
36 chr2:36608800-36611000 Weak transcription iPS-15b Cell Line embryonic stem cell
37 chr2:36608800-36611200 Weak transcription NHEK skin
38 chr2:36608800-36611400 Strong transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
39 chr2:36608800-36613000 Strong transcription Muscle Satellite Cultured Cells --
40 chr2:36608800-36613400 Strong transcription NH-A brain
41 chr2:36608800-36613600 Weak transcription Skeletal Muscle Male skeletal muscle
42 chr2:36608800-36614200 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
43 chr2:36608800-36615600 Weak transcription Fetal Adrenal Gland Adrenal Gland
44 chr2:36608800-36615600 Weak transcription Fetal Kidney kidney
45 chr2:36608800-36615600 Weak transcription Fetal Lung lung
46 chr2:36609000-36611800 Genic enhancers HepG2 liver
47 chr2:36609000-36613000 Strong transcription HSMM muscle
48 chr2:36609000-36614000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
49 chr2:36609000-36614000 Genic enhancers A549 lung
50 chr2:36609000-36615800 Weak transcription Rectal Mucosa Donor 31 rectum

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