Variant report

Variant rs4472712
Chromosome Location chr1:145211450-145211451
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:104 , 50 per page) page: 1 2 3
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:145208800-145211600 Active TSS Psoas Muscle Psoas
2 chr1:145208800-145211600 Active TSS Right Atrium heart
3 chr1:145208800-145211800 Active TSS Brain Anterior Caudate brain
4 chr1:145208800-145211800 Active TSS Brain Inferior Temporal Lobe brain
5 chr1:145208800-145211800 Active TSS Ovary ovary
6 chr1:145208800-145212200 Active TSS Brain Dorsolateral Prefrontal Cortex brain
7 chr1:145209000-145212400 Active TSS Aorta Aorta
8 chr1:145209400-145211800 Flanking Active TSS Primary B cells from cord blood blood
9 chr1:145209800-145211800 Active TSS Foreskin Fibroblast Primary Cells skin02 Skin
10 chr1:145209800-145212000 Flanking Active TSS Primary hematopoietic stem cells G-CSF-mobilized Male --
11 chr1:145210000-145211800 Flanking Active TSS Dnd41 blood
12 chr1:145210000-145212000 Flanking Active TSS Primary hematopoietic stem cells G-CSF-mobilized Female --
13 chr1:145210200-145211600 Flanking Active TSS H9 Derived Neuron Cultured Cells ES cell derived
14 chr1:145210200-145230400 Weak transcription Spleen Spleen
15 chr1:145210400-145211800 Flanking Active TSS Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
16 chr1:145210400-145211800 Flanking Active TSS Primary monocytes fromperipheralblood blood
17 chr1:145210400-145211800 Flanking Active TSS Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
18 chr1:145210400-145211800 Enhancers HepG2 liver
19 chr1:145210400-145211800 Flanking Active TSS Monocytes-CD14+_RO01746 blood
20 chr1:145210400-145215400 Weak transcription Gastric stomach
21 chr1:145210600-145211600 Active TSS Fetal Muscle Leg muscle
22 chr1:145210600-145211800 Bivalent/Poised TSS hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
23 chr1:145210600-145211800 Enhancers HUVEC blood vessel
24 chr1:145210600-145212000 Enhancers Primary T helper 17 cells PMA-I stimulated --
25 chr1:145210600-145214200 Enhancers Fetal Heart heart
26 chr1:145210600-145214600 Weak transcription Esophagus oesophagus
27 chr1:145210600-145214600 Weak transcription Sigmoid Colon Sigmoid Colon
28 chr1:145210600-145217000 Weak transcription ES-WA7 Cell Line embryonic stem cell
29 chr1:145210600-145217200 Enhancers Primary B cells from peripheral blood blood
30 chr1:145210600-145219200 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
31 chr1:145210800-145211600 Enhancers Primary T cells fromperipheralblood blood
32 chr1:145210800-145211600 Enhancers Fetal Intestine Small intestine
33 chr1:145210800-145211600 Enhancers GM12878-XiMat blood
34 chr1:145210800-145211800 Enhancers Primary T killer memory cells from peripheral blood blood
35 chr1:145210800-145211800 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
36 chr1:145210800-145211800 Enhancers Rectal Mucosa Donor 31 rectum
37 chr1:145210800-145211800 Enhancers Skeletal Muscle Female skeletal muscle
38 chr1:145210800-145211800 Enhancers Hela-S3 cervix
39 chr1:145210800-145212000 Weak transcription Pancreas Pancrea
40 chr1:145210800-145212000 Enhancers Stomach Smooth Muscle stomach
41 chr1:145210800-145212200 Enhancers Primary T regulatory cells fromperipheralblood blood
42 chr1:145210800-145212400 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
43 chr1:145210800-145212400 Enhancers Fetal Intestine Large intestine
44 chr1:145210800-145212800 Enhancers Primary T cells effector/memory enriched fromperipheralblood blood
45 chr1:145210800-145213000 Weak transcription Skeletal Muscle Male skeletal muscle
46 chr1:145210800-145213400 Weak transcription ES-I3 Cell Line embryonic stem cell
47 chr1:145210800-145213400 Enhancers A549 lung
48 chr1:145210800-145213600 Enhancers Primary T killer naive cells fromperipheralblood blood
49 chr1:145210800-145213600 Enhancers Fetal Lung lung
50 chr1:145210800-145213800 Enhancers Primary neutrophils fromperipheralblood blood

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