Variant report

Variant rs12740634
Chromosome Location chr1:62660523-62660524
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:60 , 50 per page) page: 1 2
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:62659800-62661200 Active TSS iPS-20b Cell Line embryonic stem cell
2 chr1:62659800-62661800 Active TSS iPS-18 Cell Line embryonic stem cell
3 chr1:62660000-62661000 Bivalent/Poised TSS Psoas Muscle Psoas
4 chr1:62660000-62661600 Active TSS ES-I3 Cell Line embryonic stem cell
5 chr1:62660000-62661800 Active TSS H9 Cell Line embryonic stem cell
6 chr1:62660000-62662000 Active TSS HUES48 Cell Line embryonic stem cell
7 chr1:62660000-62662000 Active TSS HUES64 Cell Line embryonic stem cell
8 chr1:62660000-62662000 Active TSS iPS DF 6.9 Cell Line embryonic stem cell
9 chr1:62660000-62662400 Active TSS hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
10 chr1:62660000-62662600 Active TSS Colonic Mucosa Colon
11 chr1:62660000-62665200 Active TSS H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
12 chr1:62660200-62660600 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
13 chr1:62660200-62660600 Flanking Bivalent TSS/Enh Primary monocytes fromperipheralblood blood
14 chr1:62660200-62660600 Flanking Active TSS Foreskin Keratinocyte Primary Cells skin02 Skin
15 chr1:62660200-62660600 Flanking Active TSS Foreskin Melanocyte Primary Cells skin03 Skin
16 chr1:62660200-62660800 Active TSS Fetal Lung lung
17 chr1:62660200-62660800 Bivalent/Poised TSS Fetal Stomach stomach
18 chr1:62660200-62661000 Flanking Active TSS Foreskin Keratinocyte Primary Cells skin03 Skin
19 chr1:62660200-62661000 Active TSS Rectal Mucosa Donor 29 rectum
20 chr1:62660200-62661000 ZNF genes & repeats Spleen Spleen
21 chr1:62660200-62661200 Active TSS hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
22 chr1:62660200-62661200 Bivalent/Poised TSS Fetal Intestine Large intestine
23 chr1:62660200-62661400 Active TSS Rectal Mucosa Donor 31 rectum
24 chr1:62660200-62662000 Active TSS H1 Cell Line embryonic stem cell
25 chr1:62660200-62662000 Active TSS iPS-15b Cell Line embryonic stem cell
26 chr1:62660200-62662000 Active TSS ES-UCSF4 Cell Line embryonic stem cell
27 chr1:62660400-62660600 Flanking Bivalent TSS/Enh Primary hematopoietic stem cells G-CSF-mobilized Male --
28 chr1:62660400-62660600 Bivalent Enhancer Cortex derived primary cultured neurospheres brain
29 chr1:62660400-62660600 Flanking Bivalent TSS/Enh Esophagus oesophagus
30 chr1:62660400-62660600 Flanking Bivalent TSS/Enh Fetal Muscle Leg muscle
31 chr1:62660400-62660600 Bivalent/Poised TSS Fetal Thymus thymus
32 chr1:62660400-62660600 Strong transcription Right Atrium heart
33 chr1:62660400-62660600 Flanking Active TSS Right Ventricle heart
34 chr1:62660400-62660600 Bivalent Enhancer Sigmoid Colon Sigmoid Colon
35 chr1:62660400-62660600 Active TSS HMEC breast
36 chr1:62660400-62660800 Active TSS HUES6 Cell Line embryonic stem cell
37 chr1:62660400-62660800 Flanking Bivalent TSS/Enh Primary hematopoietic stem cells G-CSF-mobilized Female --
38 chr1:62660400-62660800 Bivalent/Poised TSS Fetal Muscle Trunk muscle
39 chr1:62660400-62660800 Flanking Bivalent TSS/Enh Monocytes-CD14+_RO01746 blood
40 chr1:62660400-62660800 Bivalent Enhancer NH-A brain
41 chr1:62660400-62661000 Active TSS ES-WA7 Cell Line embryonic stem cell
42 chr1:62660400-62661000 Transcr. at gene 5' and 3' iPS DF 19.11 Cell Line embryonic stem cell
43 chr1:62660400-62661000 Flanking Bivalent TSS/Enh Breast Myoepithelial Primary Cells Breast
44 chr1:62660400-62661000 Bivalent/Poised TSS Foreskin Fibroblast Primary Cells skin01 Skin
45 chr1:62660400-62661000 Flanking Bivalent TSS/Enh Foreskin Melanocyte Primary Cells skin01 Skin
46 chr1:62660400-62661000 Bivalent Enhancer Brain Inferior Temporal Lobe brain
47 chr1:62660400-62661000 Flanking Bivalent TSS/Enh Fetal Adrenal Gland Adrenal Gland
48 chr1:62660400-62661000 Enhancers Fetal Heart heart
49 chr1:62660400-62661000 Flanking Active TSS Placenta Placenta
50 chr1:62660400-62661000 Bivalent/Poised TSS Stomach Smooth Muscle stomach

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